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Items: 2

1.

rs13382811 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A,T [Show Flanks]
    Chromosome:
    2:144466053 (GRCh38)
    2:145223620 (GRCh37)
    Canonical SPDI:
    NC_000002.12:144466052:C:A,NC_000002.12:144466052:C:T
    Gene:
    ZEB2 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.140676/28275 (ALFA)
    T=0.1/4 (GENOME_DK)
    T=0.101852/22 (Qatari)
    T=0.113393/508 (Estonian)
    T=0.125/75 (NorthernSweden)
    T=0.141412/545 (ALSPAC)
    T=0.148297/148 (GoNL)
    T=0.153722/570 (TWINSUK)
    T=0.184183/347 (HapMap)
    T=0.184211/14 (PRJEB36033)
    T=0.191589/41 (Vietnamese)
    T=0.210653/439 (HGDP_Stanford)
    T=0.212884/29820 (GnomAD)
    T=0.218274/172 (PRJEB37584)
    T=0.225543/59699 (TOPMED)
    T=0.228435/1144 (1000Genomes)
    T=0.271672/796 (KOREAN)
    T=0.276201/506 (Korea1K)
    T=0.279833/4690 (TOMMO)
    T=0.300319/188 (Chileans)
    C=0.307692/8 (Siberian)
    C=0.415094/88 (SGDP_PRJ)
    HGVS:
    2.

    rs60925273 has merged into rs13382811 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>A,T [Show Flanks]
      Chromosome:
      2:144466053 (GRCh38)
      2:145223620 (GRCh37)
      Canonical SPDI:
      NC_000002.12:144466052:C:A,NC_000002.12:144466052:C:T
      Gene:
      ZEB2 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.140676/28275 (ALFA)
      T=0.1/4 (GENOME_DK)
      T=0.101852/22 (Qatari)
      T=0.113393/508 (Estonian)
      T=0.125/75 (NorthernSweden)
      T=0.141412/545 (ALSPAC)
      T=0.148297/148 (GoNL)
      T=0.153722/570 (TWINSUK)
      T=0.184183/347 (HapMap)
      T=0.184211/14 (PRJEB36033)
      T=0.191589/41 (Vietnamese)
      T=0.210653/439 (HGDP_Stanford)
      T=0.212884/29820 (GnomAD)
      T=0.218274/172 (PRJEB37584)
      T=0.225543/59699 (TOPMED)
      T=0.228435/1144 (1000Genomes)
      T=0.271672/796 (KOREAN)
      T=0.276201/506 (Korea1K)
      T=0.279833/4690 (TOMMO)
      T=0.300319/188 (Chileans)
      C=0.307692/8 (Siberian)
      C=0.415094/88 (SGDP_PRJ)
      HGVS:

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