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1.

rs1107123 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C,G [Show Flanks]
    Chromosome:
    2:215796690 (GRCh38)
    2:216661413 (GRCh37)
    Canonical SPDI:
    NC_000002.12:215796689:T:C,NC_000002.12:215796689:T:G
    Gene:
    LINC00607 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.22671/45609 (ALFA)
    C=0.125/5 (GENOME_DK)
    C=0.18192/815 (Estonian)
    C=0.192385/192 (GoNL)
    C=0.195/117 (NorthernSweden)
    C=0.205882/14 (PRJEB36033)
    C=0.208468/773 (TWINSUK)
    C=0.210431/811 (ALSPAC)
    C=0.212963/46 (Qatari)
    C=0.230212/47211 (GENOGRAPHIC)
    C=0.243277/36276 (GnomAD_genomes)
    C=0.25452/67369 (TOPMED)
    C=0.287852/327 (Daghestan)
    C=0.30356/1944 (1000Genomes_30X)
    C=0.311901/1562 (1000Genomes)
    C=0.327696/620 (HapMap)
    T=0.33/99 (SGDP_PRJ)
    C=0.34405/717 (HGDP_Stanford)
    T=0.416667/10 (Siberian)
    T=0.455631/1335 (KOREAN)
    T=0.462676/3347 (Korea4K)
    T=0.46452/851 (Korea1K)
    T=0.479042/37098 (TOMMO)
    T=0.481308/103 (Vietnamese)
    HGVS:

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