[go: up one dir, main page]
U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Search results

Items: 2

1.

rs112815771 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C,G [Show Flanks]
    Chromosome:
    1:127269 (GRCh38)
    1:127269 (GRCh37)
    Canonical SPDI:
    NC_000001.11:127268:T:C,NC_000001.11:127268:T:G
    Gene:
    LOC124900384 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.14366/2346 (ALFA)
    C=0.24453/1566 (1000Genomes)
    C=0.38003/6369 (TOMMO)
    C=0.40781/1190 (KOREAN)
    T=0.5/62 (SGDP_PRJ)
    HGVS:

    2.

    rs201860035 has merged into rs112815771 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C,G [Show Flanks]
      Chromosome:
      1:127269 (GRCh38)
      1:127269 (GRCh37)
      Canonical SPDI:
      NC_000001.11:127268:T:C,NC_000001.11:127268:T:G
      Gene:
      LOC124900384 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.14366/2346 (ALFA)
      C=0.24453/1566 (1000Genomes)
      C=0.38003/6369 (TOMMO)
      C=0.40781/1190 (KOREAN)
      T=0.5/62 (SGDP_PRJ)
      HGVS:

      Supplemental Content

      Filters: Manage Filters

      Find related data

      Search details

      See more...

      Recent activity

      Clear Turn Off Turn On

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...