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1.

rs4862662 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>T [Show Flanks]
    Chromosome:
    4:186197508 (GRCh38)
    4:187118662 (GRCh37)
    Canonical SPDI:
    NC_000004.12:186197507:G:T
    Gene:
    CYP4V2 (Varview)
    Functional Consequence:
    intron_variant
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.3838684/100519 (ALFA)
    T=0.2811502/176 (Chileans)
    T=0.2824074/61 (Qatari)
    T=0.2936681/538 (Korea1K)
    T=0.2949367/233 (PRJEB37584)
    T=0.2992257/2164 (Korea4K)
    T=0.311901/1562 (1000Genomes)
    T=0.3129693/917 (KOREAN)
    T=0.3157402/2022 (1000Genomes_30X)
    T=0.3305085/624 (HapMap)
    T=0.3359331/26016 (TOMMO)
    T=0.341076/26842 (PAGE_STUDY)
    T=0.3431499/41563 (ExAC)
    G=0.34375/11 (Siberian)
    T=0.3483146/186 (MGP)
    T=0.3701802/97983 (TOPMED)
    T=0.3777433/56317 (GnomAD_genomes)
    T=0.379694/531280 (GnomAD_exomes)
    G=0.3873239/110 (SGDP_PRJ)
    T=0.3922036/5101 (GoESP)
    T=0.3930981/1515 (ALSPAC)
    T=0.4026187/246 (Vietnamese)
    T=0.4147321/1858 (Estonian)
    T=0.4174757/1548 (TWINSUK)
    T=0.4188377/418 (GoNL)
    T=0.4333333/260 (NorthernSweden)
    T=0.4440789/135 (FINRISK)
    T=0.4444444/24 (PRJEB36033)
    T=0.475/19 (GENOME_DK)
    HGVS:

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