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1.

rs11771443 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    7:150990599 (GRCh38)
    7:150687687 (GRCh37)
    Canonical SPDI:
    NC_000007.14:150990598:C:T
    Gene:
    NOS3 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.162626/24268 (ALFA)
    T=0.159209/22310 (GnomAD)
    T=0.161273/598 (TWINSUK)
    T=0.162325/162 (GoNL)
    T=0.164062/735 (Estonian)
    T=0.165/99 (NorthernSweden)
    T=0.172548/665 (ALSPAC)
    T=0.173154/45832 (TOPMED)
    T=0.185185/40 (Qatari)
    T=0.205603/389 (HapMap)
    T=0.224241/1123 (1000Genomes)
    T=0.225/9 (GENOME_DK)
    C=0.371324/101 (SGDP_PRJ)
    C=0.375/12 (Siberian)
    T=0.397196/85 (Vietnamese)
    T=0.434177/343 (PRJEB37584)
    T=0.443345/1299 (KOREAN)
    T=0.456878/837 (Korea1K)
    T=0.492004/8245 (TOMMO)
    HGVS:

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