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1.

rs537766086 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    12:6534561 (GRCh38)
    12:6643727 (GRCh37)
    Canonical SPDI:
    NC_000012.12:6534560:C:T
    Gene:
    GAPDH (Varview), LOC112268089 (Varview)
    Functional Consequence:
    genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant
    Validated:
    by frequency,by cluster
    MAF:
    T=0.0004/2 (1000Genomes)
    HGVS:

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