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1.

rs7903146 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G,T [Show Flanks]
    Chromosome:
    10:112998590 (GRCh38)
    10:114758349 (GRCh37)
    Canonical SPDI:
    NC_000010.11:112998589:C:G,NC_000010.11:112998589:C:T
    Gene:
    TCF7L2 (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Clinical significance:
    risk-factor,likely-risk-allele
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.286983/98365 (ALFA)
    T=0.024744/179 (Korea4K)
    T=0.028384/52 (Korea1K)
    T=0.028747/84 (KOREAN)
    T=0.041878/33 (PRJEB37584)
    T=0.046296/10 (Vietnamese)
    T=0.047002/3640 (TOMMO)
    T=0.170427/559 (PRJEB37766)
    T=0.198214/888 (Estonian)
    T=0.225/135 (NorthernSweden)
    T=0.227835/1141 (1000Genomes)
    T=0.231106/1480 (1000Genomes_30X)
    T=0.240466/454 (HapMap)
    T=0.241843/504 (HGDP_Stanford)
    T=0.246538/19403 (PAGE_STUDY)
    T=0.273415/40711 (GnomAD_genomes)
    T=0.276542/73198 (TOPMED)
    T=0.281563/281 (GoNL)
    T=0.285599/1059 (TWINSUK)
    T=0.297094/1145 (ALSPAC)
    T=0.3/12 (GENOME_DK)
    T=0.333333/4 (PRJEB36033)
    T=0.393519/85 (Qatari)
    C=0.39604/80 (SGDP_PRJ)
    C=0.45/9 (Siberian)
    HGVS:

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