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1.

rs751193190 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    1:55043919 (GRCh38)
    1:55509592 (GRCh37)
    Canonical SPDI:
    NC_000001.11:55043918:C:T
    Gene:
    PCSK9 (Varview)
    Functional Consequence:
    intron_variant,coding_sequence_variant,missense_variant
    Validated:
    by frequency,by cluster
    MAF:
    T=0.000004/1 (GnomAD_exomes)
    T=0.000008/1 (ExAC)
    HGVS:

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