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1.

rs1855025 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    6:167124106 (GRCh38)
    6:167537594 (GRCh37)
    Canonical SPDI:
    NC_000006.12:167124105:A:G
    Gene:
    CCR6 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.465043/92431 (ALFA)
    A=0.318182/7 (Siberian)
    G=0.324814/610 (HapMap)
    A=0.338323/113 (SGDP_PRJ)
    G=0.342593/74 (Qatari)
    G=0.363208/77 (Vietnamese)
    G=0.365697/28321 (TOMMO)
    G=0.3693/2365 (1000Genomes_30X)
    G=0.373203/1869 (1000Genomes)
    G=0.399082/105633 (TOPMED)
    G=0.399754/59577 (GnomAD_genomes)
    G=0.404762/34 (PRJEB36033)
    G=0.417406/1223 (KOREAN)
    G=0.419897/325 (PRJEB37584)
    G=0.424184/884 (HGDP_Stanford)
    G=0.426044/3082 (Korea4K)
    G=0.430131/788 (Korea1K)
    G=0.472496/1821 (ALSPAC)
    A=0.475/19 (GENOME_DK)
    A=0.485972/485 (GoNL)
    G=0.489482/1815 (TWINSUK)
    G=0.490402/2197 (Estonian)
    G=0.495/297 (NorthernSweden)
    HGVS:

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