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1.

rs7135740 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>T [Show Flanks]
    Chromosome:
    12:91106225 (GRCh38)
    12:91500002 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91106224:A:T
    Gene:
    LUM (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.023928/452 (ALFA)
    T=0.014028/14 (GoNL)
    T=0.016181/60 (TWINSUK)
    T=0.020239/78 (ALSPAC)
    T=0.023148/5 (Qatari)
    T=0.024777/111 (Estonian)
    T=0.025/1 (GENOME_DK)
    T=0.025778/3615 (GnomAD)
    T=0.032064/8487 (TOPMED)
    T=0.04/24 (NorthernSweden)
    T=0.060976/20 (HapMap)
    T=0.081043/406 (1000Genomes)
    T=0.193326/3240 (TOMMO)
    T=0.226962/665 (KOREAN)
    T=0.234716/430 (Korea1K)
    A=0.333333/2 (Siberian)
    T=0.341121/73 (Vietnamese)
    A=0.431818/57 (SGDP_PRJ)
    HGVS:

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