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Items: 2

1.

rs5751876 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    22:24441333 (GRCh38)
    22:24837301 (GRCh37)
    Canonical SPDI:
    NC_000022.11:24441332:T:C
    Gene:
    ADORA2A (Varview), ADORA2A-AS1 (Varview), SPECC1L-ADORA2A (Varview)
    Functional Consequence:
    coding_sequence_variant,non_coding_transcript_variant,intron_variant,synonymous_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.421958/14712 (ALFA)
    C=0.031835/17 (MGP)
    T=0.23913/11 (Siberian)
    C=0.305328/149 (Vietnamese)
    T=0.339806/140 (SGDP_PRJ)
    T=0.36875/1652 (Estonian)
    T=0.392839/1514 (ALSPAC)
    T=0.398867/1479 (TWINSUK)
    T=0.40625/117 (FINRISK)
    T=0.408333/245 (NorthernSweden)
    T=0.41984/419 (GoNL)
    T=0.438865/804 (Korea1K)
    C=0.442292/2215 (1000Genomes)
    T=0.442321/1296 (KOREAN)
    T=0.454741/50680 (ExAC)
    T=0.456152/107650 (GnomAD_exomes)
    T=0.467593/101 (Qatari)
    C=0.472136/7913 (TOMMO)
    T=0.476773/66794 (GnomAD)
    T=0.479674/126965 (TOPMED)
    T=0.481929/6267 (GoESP)
    HGVS:
    2.

    rs17851062 has merged into rs5751876 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      22:24441333 (GRCh38)
      22:24837301 (GRCh37)
      Canonical SPDI:
      NC_000022.11:24441332:T:C
      Gene:
      ADORA2A (Varview), ADORA2A-AS1 (Varview), SPECC1L-ADORA2A (Varview)
      Functional Consequence:
      coding_sequence_variant,non_coding_transcript_variant,intron_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.421958/14712 (ALFA)
      C=0.031835/17 (MGP)
      T=0.23913/11 (Siberian)
      C=0.305328/149 (Vietnamese)
      T=0.339806/140 (SGDP_PRJ)
      T=0.36875/1652 (Estonian)
      T=0.392839/1514 (ALSPAC)
      T=0.398867/1479 (TWINSUK)
      T=0.40625/117 (FINRISK)
      T=0.408333/245 (NorthernSweden)
      T=0.41984/419 (GoNL)
      T=0.438865/804 (Korea1K)
      C=0.442292/2215 (1000Genomes)
      T=0.442321/1296 (KOREAN)
      T=0.454741/50680 (ExAC)
      T=0.456152/107650 (GnomAD_exomes)
      T=0.467593/101 (Qatari)
      C=0.472136/7913 (TOMMO)
      T=0.476773/66794 (GnomAD)
      T=0.479674/126965 (TOPMED)
      T=0.481929/6267 (GoESP)
      HGVS:

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