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Items: 2

1.

rs3759223 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    12:91113006 (GRCh38)
    12:91506783 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91113005:A:G
    Gene:
    LUM (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.024755/586 (ALFA)
    G=0.014028/14 (GoNL)
    G=0.016721/62 (TWINSUK)
    G=0.020498/79 (ALSPAC)
    G=0.025/1 (GENOME_DK)
    G=0.025/112 (Estonian)
    G=0.026085/3657 (GnomAD)
    G=0.026683/5472 (GENOGRAPHIC)
    G=0.027778/6 (Qatari)
    G=0.032287/8546 (TOPMED)
    G=0.04/24 (NorthernSweden)
    G=0.059105/37 (Chileans)
    G=0.075212/142 (HapMap)
    G=0.081824/410 (1000Genomes)
    G=0.193255/3239 (TOMMO)
    G=0.22628/663 (KOREAN)
    G=0.235262/431 (Korea1K)
    G=0.263959/208 (PRJEB37584)
    G=0.327103/70 (Vietnamese)
    A=0.333333/2 (Siberian)
    A=0.425373/57 (SGDP_PRJ)
    HGVS:
    2.

    rs61630578 has merged into rs3759223 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      12:91113006 (GRCh38)
      12:91506783 (GRCh37)
      Canonical SPDI:
      NC_000012.12:91113005:A:G
      Gene:
      LUM (Varview)
      Functional Consequence:
      upstream_transcript_variant,2KB_upstream_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0.024755/586 (ALFA)
      G=0.014028/14 (GoNL)
      G=0.016721/62 (TWINSUK)
      G=0.020498/79 (ALSPAC)
      G=0.025/1 (GENOME_DK)
      G=0.025/112 (Estonian)
      G=0.026085/3657 (GnomAD)
      G=0.026683/5472 (GENOGRAPHIC)
      G=0.027778/6 (Qatari)
      G=0.032287/8546 (TOPMED)
      G=0.04/24 (NorthernSweden)
      G=0.059105/37 (Chileans)
      G=0.075212/142 (HapMap)
      G=0.081824/410 (1000Genomes)
      G=0.193255/3239 (TOMMO)
      G=0.22628/663 (KOREAN)
      G=0.235262/431 (Korea1K)
      G=0.263959/208 (PRJEB37584)
      G=0.327103/70 (Vietnamese)
      A=0.333333/2 (Siberian)
      A=0.425373/57 (SGDP_PRJ)
      HGVS:

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