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1.

rs221 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    7:101381867 (GRCh38)
    7:101025148 (GRCh37)
    Canonical SPDI:
    NC_000007.14:101381866:C:T
    Gene:
    COL26A1 (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.424087/8011 (ALFA)
    T=0.262195/86 (HapMap)
    T=0.290476/61 (Vietnamese)
    T=0.296819/2146 (Korea4K)
    T=0.298635/875 (KOREAN)
    T=0.306223/561 (Korea1K)
    C=0.310976/102 (SGDP_PRJ)
    T=0.323976/25090 (TOMMO)
    C=0.325/13 (Siberian)
    T=0.332136/2127 (1000Genomes_30X)
    T=0.335264/1679 (1000Genomes)
    T=0.363701/96268 (TOPMED)
    T=0.375304/55819 (GnomAD_genomes)
    T=0.421296/91 (Qatari)
    C=0.45/18 (GENOME_DK)
    T=0.466667/280 (NorthernSweden)
    T=0.483913/1865 (ALSPAC)
    T=0.486974/486 (GoNL)
    T=0.487179/38 (PRJEB36033)
    C=0.488839/2190 (Estonian)
    T=0.494067/1832 (TWINSUK)
    HGVS:

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