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Items: 1 to 20 of 36

1.

rs17239726 [Homo sapiens]
    ATCCTAATTGTATTAAGTGGTGCAC[A/G]TCCTCAATGATGTAGTTTTAAAATT
    Chromosome:
    9:115009233
    Validated:
    by 1000G,by cluster,by frequency,by hapmap
    Global MAF:
    A=0.1380/691
    HGVS:
    NC_000009.11:g.117771512G>A, NC_000009.12:g.115009233G>A
    3.

    rs12555312 [Homo sapiens]
      caaacacagtgctgggactacaaga[C/G/T]ggtcaataaatgtCACAGGCTCATG
      Chromosome:
      9:115017375
      Validated:
      by 1000G,by cluster,by frequency,by hapmap
      Global MAF:
      C=0.0805/403
      HGVS:
      NC_000009.11:g.117779654G>C, NC_000009.12:g.115017375G>C, NC_000009.12:g.115017375G>T
      5.

      rs12156617 [Homo sapiens]
        ctgggttcctactgactcctgaaac[C/T]tcatcttccacAATGCATCTTTTGC
        Chromosome:
        9:115016064
        Validated:
        by 1000G,by cluster,by frequency,by hapmap
        Global MAF:
        T=0.1300/651
        HGVS:
        NC_000009.11:g.117778343C>T, NC_000009.12:g.115016064C>T
        7.

        rs11787664 [Homo sapiens]
          GGGGACTGCAGTGTAGAGGAGAAGG[C/T]GATATTCCTAATAGACATTCTTCCT
          Chromosome:
          9:115019377
          Gene:
          TNC (GeneView)
          Functional Consequence:
          downstream variant 500B
          Validated:
          by 1000G,by cluster,by frequency,by hapmap
          Global MAF:
          T=0.3480/1743
          HGVS:
          NC_000009.11:g.117781656C>T, NC_000009.12:g.115019377C>T, NG_029637.1:g.103881G>A, NM_002160.3:c.*1780G>A
          8.

          rs10817691 [Homo sapiens]
            CTAAAATCTGGACAGGAGGGTAGGA[A/C]CTGGTACCTTGGGCCAGGCAGCTTG
            Chromosome:
            9:114957982
            Validated:
            by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
            Global MAF:
            C=0.4840/2424
            HGVS:
            NC_000009.11:g.117720262A>C, NC_000009.12:g.114957982A>C
            10.

            rs10117421 [Homo sapiens]
              tcatcttccacAATGCATCTTTTGC[A/C]CCTATGCCTCTGGCTTTCTCTGTGC
              Chromosome:
              9:115016090
              Validated:
              by 1000G,by cluster,by frequency,by hapmap
              Global MAF:
              C=0.1212/607
              HGVS:
              NC_000009.11:g.117778369A>C, NC_000009.12:g.115016090A>C
              12.

              rs4978617 [Homo sapiens]
                TGCCAGGAAAAGCCACTTCACAGGA[C/T]GCTGCAGTAATATCAGGCAGCTCCC
                Chromosome:
                9:115002569
                Validated:
                by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                Global MAF:
                C=0.4353/2180
                HGVS:
                NC_000009.11:g.117764849C>T, NC_000009.12:g.115002569C>T
                13.

                rs4452883 [Homo sapiens]
                  gttttctacatgacatggaatagtt[C/T]gatttgtctcacaggtgactatgat
                  Chromosome:
                  9:115017295
                  Validated:
                  by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                  Global MAF:
                  T=0.1546/774
                  HGVS:
                  NC_000009.11:g.117779574C>T, NC_000009.12:g.115017295C>T
                  16.

                  rs3789867 [Homo sapiens]
                    ATCATGCCATTTAGTCAACCATAGC[A/G/T]TCTAGTAAGTCTTATCACCCACCCT
                    Chromosome:
                    9:115113409
                    Gene:
                    TNC (GeneView)
                    Functional Consequence:
                    intron variant
                    Validated:
                    by 1000G,by cluster,by frequency,by hapmap
                    Global MAF:
                    C=0.3950/1978
                    HGVS:
                    NC_000009.11:g.117875688A>C, NC_000009.12:g.115113409A>C, NC_000009.12:g.115113409A>T, NG_029637.1:g.9849T>A, NG_029637.1:g.9849T>G, NM_002160.3:c.-137+4573T>A, NM_002160.3:c.-137+4573T>G, XM_005251972.1:c.-137+4573T>G, XM_005251972.3:c.-137+4573T>A, XM_005251972.3:c.-137+4573T>G, XM_005251973.1:c.-137+4573T>G, XM_005251973.3:c.-137+4573T>A, XM_005251973.3:c.-137+4573T>G, XM_005251974.1:c.-137+4573T>G, XM_005251974.3:c.-137+4573T>A, XM_005251974.3:c.-137+4573T>G, XM_005251975.1:c.-137+4573T>G, XM_005251975.3:c.-137+4573T>A, XM_005251975.3:c.-137+4573T>G, XM_006717096.3:c.-137+4573T>A, XM_006717096.3:c.-137+4573T>G, XM_006717097.3:c.-137+4573T>A, XM_006717097.3:c.-137+4573T>G, XM_006717098.3:c.-137+4573T>A, XM_006717098.3:c.-137+4573T>G, XM_006717101.3:c.-137+4573T>A, XM_006717101.3:c.-137+4573T>G, XM_011518625.2:c.-137+4573T>A, XM_011518625.2:c.-137+4573T>G, XM_011518626.2:c.-137+4573T>A, XM_011518626.2:c.-137+4573T>G, XM_011518628.2:c.-137+4573T>A, XM_011518628.2:c.-137+4573T>G, XM_011518629.2:c.-137+4573T>A, XM_011518629.2:c.-137+4573T>G, XM_017014678.1:c.-137+4573T>A, XM_017014678.1:c.-137+4573T>G, XM_017014679.1:c.-137+4573T>A, XM_017014679.1:c.-137+4573T>G, XM_017014680.1:c.-137+4573T>A, XM_017014680.1:c.-137+4573T>G, XM_017014681.1:c.-137+4573T>A, XM_017014681.1:c.-137+4573T>G
                    17.

                    rs3748166 [Homo sapiens]
                      TAATTACAAAACATATGGGGTTTTT[C/G/T]TTTCCACCGCTGGAAAAAAAAGGAG
                      Chromosome:
                      9:115117870
                      Gene:
                      TNC (GeneView)
                      Functional Consequence:
                      intron variant
                      Validated:
                      by 1000G,by cluster,by frequency,by hapmap
                      Global MAF:
                      G=0.2654/1329
                      HGVS:
                      NC_000009.11:g.117880149A>G, NC_000009.12:g.115117870A>C, NC_000009.12:g.115117870A>G, NG_029637.1:g.5388T>C, NG_029637.1:g.5388T>G, NM_002160.3:c.-137+112T>C, NM_002160.3:c.-137+112T>G, XM_005251972.1:c.-137+112T>C, XM_005251972.3:c.-137+112T>C, XM_005251972.3:c.-137+112T>G, XM_005251973.1:c.-137+112T>C, XM_005251973.3:c.-137+112T>C, XM_005251973.3:c.-137+112T>G, XM_005251974.1:c.-137+112T>C, XM_005251974.3:c.-137+112T>C, XM_005251974.3:c.-137+112T>G, XM_005251975.1:c.-137+112T>C, XM_005251975.3:c.-137+112T>C, XM_005251975.3:c.-137+112T>G, XM_006717096.3:c.-137+112T>C, XM_006717096.3:c.-137+112T>G, XM_006717097.3:c.-137+112T>C, XM_006717097.3:c.-137+112T>G, XM_006717098.3:c.-137+112T>C, XM_006717098.3:c.-137+112T>G, XM_006717101.3:c.-137+112T>C, XM_006717101.3:c.-137+112T>G, XM_011518625.2:c.-137+112T>C, XM_011518625.2:c.-137+112T>G, XM_011518626.2:c.-137+112T>C, XM_011518626.2:c.-137+112T>G, XM_011518628.2:c.-137+112T>C, XM_011518628.2:c.-137+112T>G, XM_011518629.2:c.-137+112T>C, XM_011518629.2:c.-137+112T>G, XM_017014678.1:c.-137+112T>C, XM_017014678.1:c.-137+112T>G, XM_017014679.1:c.-137+112T>C, XM_017014679.1:c.-137+112T>G, XM_017014680.1:c.-137+112T>C, XM_017014680.1:c.-137+112T>G, XM_017014681.1:c.-137+112T>C, XM_017014681.1:c.-137+112T>G
                      19.

                      rs2873892 [Homo sapiens]
                        ATGGTGTCATCGAAATGTCATACTC[A/C/G]GTAGCTTCTGGTAATTTGAAAGAAC
                        Chromosome:
                        8:139234730
                        Validated:
                        by 1000G,by cluster,by frequency,by hapmap
                        Global MAF:
                        A=0.2043/1023
                        HGVS:
                        NC_000008.10:g.140246973G>A, NC_000008.10:g.140246973G>C, NC_000008.11:g.139234730G>A, NC_000008.11:g.139234730G>C

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