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1.

rs1553687 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A [Show Flanks]
    Chromosome:
    17:53658642 (GRCh38)
    17:51736003 (GRCh37)
    Canonical SPDI:
    NC_000017.11:53658641:T:A
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.158867/3001 (ALFA)
    A=0.093333/56 (NorthernSweden)
    A=0.12055/447 (TWINSUK)
    A=0.125/5 (GENOME_DK)
    A=0.125065/482 (ALSPAC)
    A=0.127679/572 (Estonian)
    A=0.143193/1035 (Korea4K)
    A=0.145742/267 (Korea1K)
    A=0.147502/431 (KOREAN)
    A=0.168857/13077 (TOMMO)
    A=0.175195/26070 (GnomAD_genomes)
    A=0.179281/47454 (TOPMED)
    A=0.198682/995 (1000Genomes)
    A=0.198782/1273 (1000Genomes_30X)
    A=0.328704/71 (Qatari)
    T=0.404494/72 (SGDP_PRJ)
    T=0.5/12 (Siberian)
    HGVS:

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