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1.

rs3823342 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A,C [Show Flanks]
    Chromosome:
    6:29945290 (GRCh38)
    6:29913067 (GRCh37)
    Canonical SPDI:
    NC_000006.12:29945289:T:A,NC_000006.12:29945289:T:C
    Gene:
    HLA-A (Varview), LOC124901298 (Varview)
    Functional Consequence:
    intron_variant,non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.494736/52439 (ALFA)
    C=0.235955/126 (MGP)
    C=0.29672/184911 (GnomAD_exomes)
    T=0.319512/131 (SGDP_PRJ)
    T=0.35/14 (GENOME_DK)
    T=0.37037/80 (Qatari)
    T=0.380952/16 (Siberian)
    T=0.403333/242 (NorthernSweden)
    T=0.406485/1191 (KOREAN)
    T=0.412556/2760 (Korea4K)
    T=0.444493/34770 (PAGE_STUDY)
    T=0.466093/35369 (TOMMO)
    T=0.469287/56688 (ExAC)
    T=0.469848/2353 (1000Genomes)
    C=0.495992/495 (GoNL)
    T=0.497403/383 (PRJEB37584)
    HGVS:
    NC_000006.12:g.29945290T>A, NC_000006.12:g.29945290T>C, NC_000006.11:g.29913067T>A, NC_000006.11:g.29913067T>C, NG_029217.3:g.7760T>A, NG_029217.3:g.7760T>C, NG_029217.2:g.7826T>A, NG_029217.2:g.7826T>C, NT_113891.3:g.1424713T>A, NT_113891.3:g.1424713T>C, NT_113891.2:g.1424819T>A, NT_113891.2:g.1424819T>C, NT_167244.2:g.1203038T>A, NT_167244.2:g.1203038T>C, NW_003871063.1:g.179215T>A, NW_003871063.1:g.179215T>C, NT_167248.2:g.1200264C>T, NT_167248.2:g.1200264C>A, NT_167248.1:g.1205860C>T, NT_167248.1:g.1205860C>A, NT_167245.2:g.1200858C>T, NT_167245.2:g.1200858C>A, NT_167245.1:g.1206443C>T, NT_167245.1:g.1206443C>A, NT_167249.2:g.1243120C>T, NT_167249.2:g.1243120C>A, NT_167249.1:g.1242418C>T, NT_167249.1:g.1242418C>A, NT_167246.2:g.1199848C>T, NT_167246.2:g.1199848C>A, NT_167246.1:g.1205468C>T, NT_167246.1:g.1205468C>A, NT_167247.2:g.1289385C>T, NT_167247.2:g.1289385C>A, NT_167247.1:g.1294970C>T, NT_167247.1:g.1294970C>A, NT_167244.1:g.1152954T>A, NT_167244.1:g.1152954T>C, XM_041680768.2:c.1093C>T, XM_041680768.2:c.1093C>A, XM_041680768.1:c.1093C>T, XM_041680768.1:c.1093C>A, XR_007059541.1:n.304A>T, XR_007059541.1:n.304A>G

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