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1.

rs1455837 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    2:219048036 (GRCh38)
    2:219912758 (GRCh37)
    Canonical SPDI:
    NC_000002.12:219048035:A:G
    Gene:
    LOC107985987 (Varview)
    Functional Consequence:
    non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.375282/25971 (ALFA)
    A=0.227273/10 (Siberian)
    G=0.266277/20621 (TOMMO)
    G=0.275028/1989 (Korea4K)
    G=0.275085/806 (KOREAN)
    G=0.276201/506 (Korea1K)
    G=0.277778/60 (Vietnamese)
    A=0.294643/1320 (Estonian)
    A=0.3/12 (GENOME_DK)
    A=0.308333/185 (NorthernSweden)
    A=0.335671/335 (GoNL)
    A=0.33809/1303 (ALSPAC)
    A=0.343581/1274 (TWINSUK)
    A=0.353125/113 (SGDP_PRJ)
    A=0.36/18 (PRJEB36033)
    G=0.369174/697 (HapMap)
    G=0.410369/2628 (1000Genomes_30X)
    G=0.413339/2070 (1000Genomes)
    G=0.425624/887 (HGDP_Stanford)
    A=0.481874/71857 (GnomAD_genomes)
    G=0.485817/128591 (TOPMED)
    A=0.490741/106 (Qatari)
    HGVS:

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