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Links from Gene

Items: 3

1.

rs879008433 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    NT_187368.1:7043 (GRCh38)
    NT_187368.1:-1 (GRCh37)
    Canonical SPDI:
    NT_187368.1:7042:C:T
    Gene:
    LOC102724562 (Varview)
    Functional Consequence:
    non_coding_transcript_variant
    HGVS:

    2.

    rs878995872 [Homo sapiens]
      Variant type:
      MNV
      Alleles:
      ACG>GCT [Show Flanks]
      Chromosome:
      NT_187368.1:6979 (GRCh38)
      NT_187368.1:-1 (GRCh37)
      Canonical SPDI:
      NT_187368.1:6978:ACG:GCT
      Gene:
      LOC102724562 (Varview)
      Functional Consequence:
      non_coding_transcript_variant
      HGVS:

      3.

      rs71208559 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C [Show Flanks]
        Chromosome:
        NT_187368.1:5942 (GRCh38)
        NT_187368.1:-1 (GRCh37)
        Canonical SPDI:
        NT_187368.1:5941:T:C
        Gene:
        LOC102724562 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by cluster
        HGVS:

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