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Items: 2

1.

rs1990550 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>C,T [Show Flanks]
    Chromosome:
    12:91057866 (GRCh38)
    12:91451643 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91057865:G:C,NC_000012.12:91057865:G:T
    Gene:
    KERA (Varview)
    Functional Consequence:
    5_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.034913/274 (ALFA)
    G=0./0 (GENOME_DK)
    G=0./0 (KOREAN)
    G=0./0 (Korea1K)
    G=0./0 (TOMMO)
    G=0.009025/5 (SGDP_PRJ)
    G=0.017177/86 (1000Genomes)
    G=0.017857/1 (Siberian)
    G=0.02/12 (NorthernSweden)
    G=0.028649/7583 (TOPMED)
    G=0.033036/148 (Estonian)
    G=0.041667/9 (Qatari)
    G=0.168337/168 (GoNL)
    HGVS:
    2.

    rs61330459 has merged into rs1990550 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>C,T [Show Flanks]
      Chromosome:
      12:91057866 (GRCh38)
      12:91451643 (GRCh37)
      Canonical SPDI:
      NC_000012.12:91057865:G:C,NC_000012.12:91057865:G:T
      Gene:
      KERA (Varview)
      Functional Consequence:
      5_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0.034913/274 (ALFA)
      G=0./0 (GENOME_DK)
      G=0./0 (KOREAN)
      G=0./0 (Korea1K)
      G=0./0 (TOMMO)
      G=0.009025/5 (SGDP_PRJ)
      G=0.017177/86 (1000Genomes)
      G=0.017857/1 (Siberian)
      G=0.02/12 (NorthernSweden)
      G=0.028649/7583 (TOPMED)
      G=0.033036/148 (Estonian)
      G=0.041667/9 (Qatari)
      G=0.168337/168 (GoNL)
      HGVS:

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