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1.

rs2617266 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    2:38075401 (GRCh38)
    2:38302544 (GRCh37)
    Canonical SPDI:
    NC_000002.12:38075400:G:A
    Gene:
    CYP1B1 (Varview)
    Functional Consequence:
    intron_variant
    Clinical significance:
    benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.284452/8694 (ALFA)
    A=0.109668/1838 (TOMMO)
    A=0.160837/469 (KOREAN)
    A=0.163934/300 (Korea1K)
    A=0.257551/955 (TWINSUK)
    A=0.267728/3481 (GoESP)
    A=0.26779/143 (MGP)
    A=0.270811/71681 (TOPMED)
    A=0.277115/1068 (ALSPAC)
    A=0.281143/39400 (GnomAD)
    A=0.282407/61 (Qatari)
    A=0.288726/1446 (1000Genomes)
    A=0.291583/291 (GoNL)
    A=0.292614/70960 (GnomAD_exomes)
    A=0.299282/34017 (ExAC)
    A=0.3/12 (GENOME_DK)
    A=0.349777/1567 (Estonian)
    A=0.36/216 (NorthernSweden)
    A=0.399306/115 (FINRISK)
    G=0.407407/110 (SGDP_PRJ)
    G=0.4375/14 (Siberian)
    HGVS:

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