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1.

rs7452972 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G,T [Show Flanks]
    Chromosome:
    6:4475448 (GRCh38)
    6:4475682 (GRCh37)
    Canonical SPDI:
    NC_000006.12:4475447:A:G,NC_000006.12:4475447:A:T
    Gene:
    LOC105374894 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.254156/4801 (ALFA)
    T=0.151303/151 (GoNL)
    T=0.161543/599 (TWINSUK)
    T=0.165023/636 (ALSPAC)
    T=0.171429/768 (Estonian)
    T=0.181667/109 (NorthernSweden)
    T=0.205061/1483 (Korea4K)
    T=0.207509/608 (KOREAN)
    T=0.252336/54 (Vietnamese)
    T=0.275/11 (GENOME_DK)
    T=0.281378/21791 (TOMMO)
    T=0.314534/46858 (GnomAD_genomes)
    T=0.337111/89230 (TOPMED)
    A=0.367089/116 (SGDP_PRJ)
    T=0.379992/1903 (1000Genomes)
    T=0.38273/2451 (1000Genomes_30X)
    T=0.412037/89 (Qatari)
    A=0.5/9 (Siberian)
    HGVS:

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