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1.

rs6523677 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G [Show Flanks]
    Chromosome:
    X:80013943 (GRCh38)
    X:79269442 (GRCh37)
    Canonical SPDI:
    NC_000023.11:80013942:A:C,NC_000023.11:80013942:A:G
    Gene:
    TBX22 (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.277921/11218 (ALFA)
    A=0.07377/216 (KOREAN)
    A=0.076997/402 (Korea4K)
    A=0.084113/5565 (TOMMO)
    A=0.09375/3 (Siberian)
    A=0.121951/40 (SGDP_PRJ)
    A=0.208333/10 (Vietnamese)
    C=0.275/11 (GENOME_DK)
    C=0.276566/799 (ALSPAC)
    C=0.292341/1084 (TWINSUK)
    C=0.324074/35 (Qatari)
    C=0.372738/98660 (TOPMED)
    C=0.478252/2298 (1000Genomes_30X)
    C=0.485563/1833 (1000Genomes)
    HGVS:

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