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1.

rs11568324 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    16:55692146 (GRCh38)
    16:55726058 (GRCh37)
    Canonical SPDI:
    NC_000016.10:55692145:C:T
    Gene:
    SLC6A2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.0075039/144 (ALFA)
    T=0.0001383/1 (Korea4K)
    T=0.0005459/1 (Korea1K)
    T=0.0018727/1 (MGP)
    T=0.0030303/1 (HapMap)
    T=0.0032792/21 (1000Genomes_30X)
    T=0.0035942/18 (1000Genomes)
    T=0.0047867/1267 (TOPMED)
    T=0.0053186/794 (GnomAD_genomes)
    T=0.0073661/33 (Estonian)
    T=0.0083499/10005 (GnomAD_exomes)
    T=0.0083682/4 (PharmGKB)
    T=0.0092593/2 (Qatari)
    T=0.01002/10 (GoNL)
    T=0.0101194/39 (ALSPAC)
    T=0.0105178/39 (TWINSUK)
    T=0.0116667/7 (NorthernSweden)
    C=0.5/1 (SGDP_PRJ)
    HGVS:

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