clinvar_variant_summary

• Versions: 2019-07

• Reference genome builds: GRCh37, GRCh38

• Type: hail.Table

Schema (2019-07, GRCh37)

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Global fields:
    None
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Row fields:
    'Type': str
    'Name': str
    'GeneID': int32
    'GeneSymbol': str
    'HGNC_ID': str
    'ClinicalSignificance': str
    'ClinSigSimple': int32
    'LastEvaluated': str
    'RS# (dbSNP)': int32
    'nsv/esv (dbVar)': str
    'RCVaccession': str
    'PhenotypeIDS': str
    'PhenotypeList': str
    'Origin': str
    'OriginSimple': str
    'Assembly': str
    'ChromosomeAccession': str
    'ReferenceAllele': str
    'AlternateAllele': str
    'Cytogenetic': str
    'ReviewStatus': str
    'NumberSubmitters': int32
    'Guidelines': str
    'TestedInGTR': str
    'OtherIDs': str
    'SubmitterCategories': int32
    'VariationID': int32
    'interval': interval<locus<GRCh37>>
    'AlleleID': int32
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Key: ['interval']
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