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2.

rs916864579 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    1:25883687 (GRCh38)
    1:26210178 (GRCh37)
    Canonical SPDI:
    NC_000001.11:25883686:C:T
    Gene:
    STMN1 (Varview)
    Functional Consequence:
    500B_downstream_variant,downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    T=0.000007/1 (GnomAD)
    T=0.000019/5 (TOPMED)
    HGVS:

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