Affiliation_id_name_lookup.js

[
    {
        "affiliation_id": "10000",
        "affiliation_vcep_id": "50000",
        "affiliation_fullname": "VCI Admin"
    },
    {
        "affiliation_id": "10001",
        "affiliation_vcep_id": "50001",
        "affiliation_fullname": "KCNQ1 VCEP"
    },
    {
        "affiliation_id": "10002",
        "affiliation_vcep_id": "50002",
        "affiliation_fullname": "Cardiomyopathy VCEP",
        "guideline_name": "ClinGen Cardiomyopathy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50002/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10003",
        "affiliation_fullname": "Arrhythmogenic Right Ventricular Cardiomyopathy"
    },
    {
        "affiliation_id": "10004",
        "affiliation_vcep_id": "50004",
        "affiliation_fullname": "Familial Hypercholesterolemia VCEP",
        "guideline_name": "ClinGen Familial Hypercholesterolemia Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50004/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10005",
        "affiliation_fullname": "Epilepsy"
    },
    {
        "affiliation_id": "10006",
        "affiliation_fullname": "Intellectual Disability and Autism"
    },
    {
        "affiliation_id": "10007",
        "affiliation_vcep_id": "50007",
        "affiliation_fullname": "Hearing Loss VCEP",
        "guideline_name": "ClinGen Hearing Loss Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50007/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10008",
        "affiliation_fullname": "Hypertrophic Cardiomyopathy"
    },
    {
        "affiliation_id": "10009",
        "affiliation_vcep_id": "50009",
        "affiliation_fullname": "Lysosomal Storage Disorders VCEP",
        "guideline_name": "ClinGen Lysosomal Storage Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50009/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10010",
        "affiliation_vcep_id": "50010",
        "affiliation_fullname": "Fatty Acid Oxidation Disorders VCEP"
    },
    {
        "affiliation_id": "10011",
        "affiliation_vcep_id": "50011",
        "affiliation_fullname": "Aminoacidopathy VCEP"
    },
    {
        "affiliation_id": "10012",
        "affiliation_vcep_id": "50012",
        "affiliation_fullname": "PTEN VCEP",
        "guideline_name": "ClinGen PTEN Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50012/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10013",
        "affiliation_vcep_id": "50013",
        "affiliation_fullname": "TP53 VCEP",
        "guideline_name": "ClinGen TP53 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50013/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10014",
        "affiliation_vcep_id": "50014",
        "affiliation_fullname": "CDH1 VCEP",
        "guideline_name": "ClinGen CDH1 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50014/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10015",
        "affiliation_vcep_id": "50015",
        "affiliation_fullname": "Phenylketonuria VCEP",
        "guideline_name": "ClinGen PAH Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50015/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10016",
        "affiliation_vcep_id": "50016",
        "affiliation_fullname": "Monogenic Diabetes VCEP",
        "guideline_name": "ClinGen Monogenic Diabetes Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50016/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10017",
        "affiliation_vcep_id": "50017",
        "affiliation_fullname": "Sequence Variant Discrepancy Resolution"
    },
    {
        "affiliation_id": "10018",
        "affiliation_fullname": "UNC Biocuration Core"
    },
    {
        "affiliation_id": "10019",
        "affiliation_fullname": "Harvard/Geisinger Biocuration Core"
    },
    {
        "affiliation_id": "10020",
        "affiliation_vcep_id": "50020",
        "affiliation_fullname": "Brain Malformations VCEP",
        "guideline_name": "ClinGen Brain Malformations Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50020/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10021",
        "affiliation_vcep_id": "50021",
        "affiliation_fullname": "RASopathy VCEP",
        "guideline_name": "ClinGen RASopathy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50021/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10022",
        "affiliation_vcep_id": "50022",
        "affiliation_fullname": "Rett and Angelman-like Disorders VCEP",
        "guideline_name": "ClinGen Rett and Angelman-like Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50022/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10023",
        "affiliation_fullname": "Hereditary Cancer"
    },
    {
        "affiliation_id": "10024",
        "affiliation_fullname": "BCM Education"
    },
    {
        "affiliation_id": "10025",
        "affiliation_fullname": "Long QT Syndrome"
    },
    {
        "affiliation_id": "10026",
        "affiliation_fullname": "General Gene Curation"
    },
    {
        "affiliation_id": "10027",
        "affiliation_vcep_id": "50027",
        "affiliation_fullname": "Mitochondrial Diseases VCEP",
        "guideline_name": "ClinGen Mitochondrial Disease Nuclear and Mitochondrial Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50027/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10028",
        "affiliation_fullname": "Hemostasis Thrombosis"
    },
    {
        "affiliation_id": "10029",
        "affiliation_fullname": "Broad Institute Rare Disease Group"
    },
    {
        "affiliation_id": "10031",
        "affiliation_vcep_id": "50031",
        "affiliation_fullname": "Congenital Myopathies VCEP"
    },
    {
        "affiliation_id": "10032",
        "affiliation_fullname": "Stanford Center for Inherited Cardiovascular Disease"
    },
    {
        "affiliation_id": "10033",
        "affiliation_fullname": "Germline/Somatic Variant Subcommittee"
    },
    {
        "affiliation_id": "10034",
        "affiliation_vcep_id": "50034",
        "affiliation_fullname": "Myeloid Malignancy VCEP",
        "guideline_name": "ClinGen Myeloid Malignancy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50034/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10035",
        "affiliation_fullname": "Dilated Cardiomyopathy"
    },
    {
        "affiliation_id": "10036",
        "affiliation_vcep_id": "50036",
        "affiliation_fullname": "VHL VCEP"
    },
    {
        "affiliation_id": "10037",
        "affiliation_vcep_id": "50037",
        "affiliation_fullname": "Hereditary Hemorrhagic Telangiectasia VCEP"
    },
    {
        "affiliation_id": "10038",
        "affiliation_vcep_id": "50038",
        "affiliation_fullname": "Malignant Hyperthermia Susceptibility VCEP",
        "guideline_name": "ClinGen Malignant Hyperthermia Susceptibility Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50038/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10039",
        "affiliation_vcep_id": "50039",
        "affiliation_fullname": "Hereditary Breast, Ovarian and Pancreatic Cancer VCEP",
        "guideline_name": "ClinGen Hereditary Breast, Ovarian and Pancreatic Cancer Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for ATM Version 1",
        "guideline_url": "https://clinicalgenome.org/site/assets/files/7392/clingen_hbop_acmg_specifications_atm_v1-1.pdf"
    },
    {
        "affiliation_id": "10040",
        "affiliation_vcep_id": "50040",
        "affiliation_fullname": "Platelet Disorders VCEP",
        "guideline_name": "ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50040/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10041",
        "affiliation_vcep_id": "50041",
        "affiliation_fullname": "Coagulation Factor Deficiency VCEP"
    },
    {
        "affiliation_id": "10042",
        "affiliation_fullname": "Breast/Ovarian Cancer"
    },
    {
        "affiliation_id": "10043",
        "affiliation_fullname": "Colon Cancer"
    },
    {
        "affiliation_id": "10044",
        "affiliation_fullname": "Heritable Thoracic Aortic Aneurysm and Dissection"
    },
    {
        "affiliation_id": "10045",
        "affiliation_fullname": "Brugada Syndrome"
    },
    {
        "affiliation_id": "10046",
        "affiliation_vcep_id": "50046",
        "affiliation_fullname": "FBN1 VCEP",
        "guideline_name": "ClinGen FBN1 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://clinicalgenome.org/site/assets/files/7445/clingen_fbn1_acmg_specifications_v1.pdf"
    },
    {
        "affiliation_id": "10047",
        "affiliation_vcep_id": "50047",
        "affiliation_fullname": "Cerebral Creatine Deficiency Syndromes VCEP",
        "guideline_name": "ClinGen Cerebral Creatine Deficiency Syndromes Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/site/assets/files/8258/clingen_ccds_acmg_specifications_v1-2.pdf"
    },
    {
        "affiliation_id": "10048",
        "affiliation_vcep_id": "50048",
        "affiliation_fullname": "ACADVL VCEP",
        "guideline_name": "ClinGen ACADVL Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://clinicalgenome.org/site/assets/files/7380/clingen_acadvl_acmg_specifications_v1.pdf"
    },
    {
        "affiliation_id": "10049",
        "affiliation_vcep_id": "50049",
        "affiliation_fullname": "Peroxisomal Disorders VCEP"
    },
    {
        "affiliation_id": "10050",
        "affiliation_vcep_id": "50050",
        "affiliation_fullname": "DICER1 and miRNA-Processing Gene VCEP",
        "guideline_name": "ClinGen DICER1 and miRNA-Processing Gene Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for DICER1 Version 1",
        "guideline_url": "https://www.clinicalgenome.org/site/assets/files/8147/clingen_dicer1_acmg_specifications_dicer1_v1.pdf"
    },
    {
        "affiliation_id": "10051",
        "affiliation_vcep_id": "50051",
        "affiliation_fullname": "von Willebrand Disease VCEP"
    },
    {
        "affiliation_id": "10052",
        "affiliation_vcep_id": "50052",
        "affiliation_fullname": "Hemoglobinopathy VCEP"
    },
    {
        "affiliation_id": "10053",
        "affiliation_vcep_id": "50053",
        "affiliation_fullname": "Glaucoma VCEP",
        "guideline_name": "ClinGen Glaucoma Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/50053/docs/assertion-criteria"
    },
    {
        "affiliation_id": "10054",
        "affiliation_fullname": "Myopathies"
    },
    {
        "affiliation_id": "10055",
        "affiliation_fullname": "Dosage Sensitivity"
    },
    {
        "affiliation_id": "10056",
        "affiliation_fullname": "Actionability"
    },
    {
        "affiliation_id": "10057",
        "affiliation_fullname": "Somatic Cancer"
    },
    {
        "affiliation_id": "10058",
        "affiliation_fullname": "ABCD1"
    },
    {
        "affiliation_id": "10059",
        "affiliation_fullname": "Craniofacial Malformations"
    },
    {
        "affiliation_id": "10060",
        "affiliation_fullname": "Syndromic Disorders"
    },
    {
        "affiliation_id": "10061",
        "affiliation_fullname": "Limb Girdle Muscular Dystrophy"
    },
    {
        "affiliation_id": "10062",
        "affiliation_fullname": "InSiGHT_Dev"
    },
    {
        "affiliation_id": "10063",
        "affiliation_fullname": "Charcot-Marie-Tooth"
    },
    {
        "affiliation_id": "10064",
        "affiliation_vcep_id": "50064",
        "affiliation_fullname": "Thrombosis VCEP"
    },
    {
        "affiliation_id": "10065",
        "affiliation_fullname": "Skeletal Disorders"
    },
    {
        "affiliation_id": "10066",
        "affiliation_fullname": "Kidney Cystic and Ciliopathy Disorders"
    },
    {
        "affiliation_id": "10067",
        "affiliation_fullname": "Tubulopathy"
    },
    {
        "affiliation_id": "10068",
        "affiliation_fullname": "Glomerulopathy"
    },
    {
        "affiliation_id": "10069",
        "affiliation_fullname": "Complement-Mediated Kidney Diseases"
    },
    {
        "affiliation_id": "10070",
        "affiliation_fullname": "Congenital Anomalies of the Kidney and Urinary Tract"
    },
    {
        "affiliation_id": "10071",
        "affiliation_vcep_id": "50071",
        "affiliation_fullname": "Pulmonary Hypertension VCEP"
    },
    {
        "affiliation_id": "10072",
        "affiliation_fullname": "Retina"
    },
    {
        "affiliation_id": "10073",
        "affiliation_fullname": "Reproduction and Infertility"
    },
    {
        "affiliation_id": "10074",
        "affiliation_fullname": "Catecholaminergic Polymorphic Ventricular Tachycardia"
    },
    {
        "affiliation_id": "10075",
        "affiliation_fullname": "Short QT Syndrome"
    },
    {
        "affiliation_id": "10076",
        "affiliation_fullname": "Centre for Translational Genomics - Memorial University of Newfoundland/Eastern Health"
    },
    {
        "affiliation_id": "10077",
        "affiliation_fullname": "Glaucoma and Neuro-Ophthalmology"
    },
    {
        "affiliation_id": "10078",
        "affiliation_vcep_id": "50078",
        "affiliation_fullname": "GRIN Disorders VCEP"
    },
    {
        "affiliation_id": "10079",
        "affiliation_fullname": "Parkinson's disease"
    },
    {
        "affiliation_id": "10080",
        "affiliation_fullname": "Antibody Deficiencies GCEP"
    },
    {
        "affiliation_id": "10081",
        "affiliation_fullname": "SCID-CID"
    },
    {
        "affiliation_id": "10082",
        "affiliation_vcep_id": "50082",
        "affiliation_fullname": "Leber Congenital Amaurosis/early onset Retinal Dystrophy VCEP"
    },
    {
        "affiliation_id": "10083",
        "affiliation_fullname": "Plon-Cancer Research"
    },
    {
        "affiliation_id": "10084",
        "affiliation_fullname": "Myriad Women's Health"
    },
    {
        "affiliation_id": "10085",
        "affiliation_fullname": "Illumina"
    },
    {
        "affiliation_id": "10086",
        "affiliation_vcep_id": "50086",
        "affiliation_fullname": "X-linked Inherited Retinal Disease VCEP"
    },
    {
        "affiliation_id": "10087",
        "affiliation_vcep_id": "50087",
        "affiliation_fullname": "BRCA1/BRCA2 VCEP"
    },
    {
        "affiliation_id": "10088",
        "affiliation_fullname": "National Institute of Cardiology - Brazil"
    },
    {
        "affiliation_id": "10089",
        "affiliation_fullname": "NTRK Fusions"
    },
    {
        "affiliation_id": "10090",
        "affiliation_vcep_id": "50090",
        "affiliation_fullname": "Optic Nerve Atrophy VCEP"
    },
    {
        "affiliation_id": "10091",
        "affiliation_vcep_id": "50091",
        "affiliation_fullname": "SCID VCEP"
    },
    {
        "affiliation_id": "10092",
        "affiliation_fullname": "H3Africa Rare Disease Working Group"
    },
    {
        "affiliation_id": "10093",
        "affiliation_fullname": "Grenoble-Alpes University Hospital"
    },
    {
        "affiliation_id": "10094",
        "affiliation_fullname": "Auragen"
    },
    {
        "affiliation_id": "10095",
        "affiliation_vcep_id": "50095",
        "affiliation_fullname": "Antibody Deficiencies VCEP"
    },
    {
        "affiliation_id": "10096",
        "affiliation_fullname": "Amyotrophic Lateral Sclerosis Spectrum Disorders"
    },
    {
        "affiliation_id": "10097",
        "affiliation_fullname": "General Inborn Errors of Metabolism"
    },
    {
        "affiliation_id": "10098",
        "affiliation_fullname": "Fibroblast Growth Factor Receptor Mutations"
    },
    {
        "affiliation_id": "10099",
        "affiliation_vcep_id": "50099",
        "affiliation_fullname": "InSiGHT Hereditary Colorectal Cancer/Polyposis VCEP"
    },
    {
        "affiliation_id": "10100",
        "affiliation_vcep_id": "50100",
        "affiliation_fullname": "Urea Cycle Disorders VCEP"
    },
    {
        "affiliation_id": "10101",
        "affiliation_vcep_id": "50101",
        "affiliation_fullname": "KCNQ Channel Brain Disorders VCEP"
    },
    {
        "affiliation_id": "10102",
        "affiliation_fullname": "Motile Ciliopathy"
    },
    {
        "affiliation_id": "10103",
        "affiliation_fullname": "UCT Neurology Research Group"
    },
    {
        "affiliation_id": "10104",
        "affiliation_fullname": "Hereditary Cardiovascular Disease"
    },
    {
        "affiliation_id": "10105",
        "affiliation_vcep_id": "50105",
        "affiliation_fullname": "Epilepsy Sodium Channel VCEP"
    },
    {
        "affiliation_id": "10106",
        "affiliation_fullname": "Prenatal"
    },
    {
        "affiliation_id": "10107",
        "affiliation_vcep_id": "50107",
        "affiliation_fullname": "Leukodystrophy and Leukoencephalopathy VCEP"
    },
    {
        "affiliation_id": "10108",
        "affiliation_vcep_id": "50108",
        "affiliation_fullname": "Potassium Channel Arrhythmia VCEP"
    },
    {
        "affiliation_id": "10109",
        "affiliation_fullname": "Pharmacogenomics"
    },
    {
        "affiliation_id": "10110",
        "affiliation_fullname": "Lysosomal Diseases"
    },
    {
        "affiliation_id": "10111",
        "affiliation_vcep_id": "50111",
        "affiliation_fullname": "FLT3 (Fms Related Receptor Tyrosine Kinase 3) SC-VCEP"
    },
    {
        "affiliation_id": "10112",
        "affiliation_fullname": "Ocular Genomics Institute"
    },
    {
        "affiliation_id": "10113",
        "affiliation_fullname": "Cerebral Palsy"
    },
    {
        "affiliation_id": "10114",
        "affiliation_vcep_id": "50114",
        "affiliation_fullname": "Neurofibromatosis and Schwannomatosis VCEP"
    },
    {
        "affiliation_id": "10115",
        "affiliation_vcep_id": "50115",
        "affiliation_fullname": "Histone H3 SC-VCEP"
    },
    {
        "affiliation_id": "10116",
        "affiliation_vcep_id": "50116",
        "affiliation_fullname": "Stanford Gecko Variant Curation"
    },
    {
        "affiliation_id": "10117",
        "affiliation_vcep_id": "50117",
        "affiliation_fullname": "Sample Affiliation Variant Curation"
    },
    {
        "affiliation_id": "10118",
        "affiliation_vcep_id": "50118",
        "affiliation_fullname": "DDC (Dopa Decarboxylase) VCEP"
    },
    {
        "affiliation_id": "10119",
        "affiliation_fullname": "HLA"
    },
    {
        "affiliation_id": "10120",
        "affiliation_fullname": "Rady's Children's Institute for Genomic Medicine"
    },
    {
        "affiliation_id": "10121",
        "affiliation_fullname": "Centre for Population Genomics"
    },
    {
        "affiliation_id": "10122",
        "affiliation_fullname": "Rheumatoid Arthritis"
    },
    {
        "affiliation_id": "10123",
        "affiliation_fullname": "Systemic Lupus Erythematosus"
    },
    {
        "affiliation_id": "10124",
        "affiliation_fullname": "Scleroderma"
    },
    {
        "affiliation_id": "10125",
        "affiliation_fullname": "Gout"
    },
    {
        "affiliation_id": "10126",
        "affiliation_fullname": "Ankylosing Spondylitis"
    },
    {
        "affiliation_id": "10127",
        "affiliation_fullname": "Clalit Genomics Center"
    },
    {
        "affiliation_id": "10128",
        "affiliation_vcep_id": "50128",
        "affiliation_fullname": "Hereditary Angioedema VCEP"
    },
    {
        "affiliation_id": "10129",
        "affiliation_vcep_id": "50129",
        "affiliation_fullname": "BCR::ABL1-like B-lymphoblastic Leukemia/Lymphoma SC-VCEP"
    },
    {
        "affiliation_id": "10130",
        "affiliation_fullname": "Congenital Heart Disease"
    },
    {
        "affiliation_id": "10131",
        "affiliation_fullname": "Ingles Lab - Garvan Institute Sydney"
    },
    {
        "affiliation_id": "10132",
        "affiliation_vcep_id": "50132",
        "affiliation_fullname": "Anterior Segment Dysgenesis VCEP"
    },
    {
        "affiliation_id": "10133",
        "affiliation_vcep_id": "50133",
        "affiliation_fullname": "Severe Combined Immunodeficiency Disease VCEP"
    },
    {
        "affiliation_id": "10134",
        "affiliation_fullname": "Molecular Pathology & Genetics - Mater Dei Hospital"
    },
    {
        "affiliation_id": "10135",
        "affiliation_fullname": "Congenital Disorders of Glycosylation"
    },
    {
        "affiliation_id": "10136",
        "affiliation_vcep_id": "50136",
        "affiliation_fullname": "Galactosemia VCEP"
    },
    {
        "affiliation_id": "10137",
        "affiliation_fullname": "ALSAfrica-NET biocurators"
    },
    {
        "affiliation_id": "10138",
        "affiliation_fullname": "Interstitial Lung Disease"
    },
    {
        "affiliation_id": "77777",
        "affiliation_vcep_id": "57777",
        "affiliation_fullname": "ClinGen Collaboration Test Affiliation VCEP",
        "guideline_name": "ClinGen Collaboration Test Affiliation Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
        "guideline_url": "https://www.clinicalgenome.org/affiliation/57777/docs/assertion-criteria"
    }
]