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1.

rs12507156 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    4:186195678 (GRCh38)
    4:187116832 (GRCh37)
    Canonical SPDI:
    NC_000004.12:186195677:C:T
    Gene:
    CYP4V2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.458549/8662 (ALFA)
    T=0.327511/600 (Korea1K)
    T=0.330612/2389 (Korea4K)
    C=0.339394/112 (SGDP_PRJ)
    C=0.34375/11 (Siberian)
    T=0.345051/1011 (KOREAN)
    T=0.354876/27483 (TOMMO)
    T=0.398148/86 (Qatari)
    T=0.415931/1603 (ALSPAC)
    T=0.425919/2133 (1000Genomes)
    T=0.43192/1935 (Estonian)
    T=0.434728/2784 (1000Genomes_30X)
    T=0.438242/1625 (TWINSUK)
    T=0.438679/93 (Vietnamese)
    T=0.438878/438 (GoNL)
    T=0.465/279 (NorthernSweden)
    T=0.475/19 (GENOME_DK)
    T=0.476812/70962 (GnomAD_genomes)
    T=0.482054/127595 (TOPMED)
    HGVS:

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