Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 32

1.

rs17782313 [Homo sapiens]
    GTTTAAAGCAGGAGAGATTGTATCC[C/T]GATGGAAATGACAAGAAAAGCTTCA
    Chromosome:
    18:60183864
    Clinical significance:
    drug-response
    Validated:
    by 1000G,by cluster,by frequency,by hapmap
    Global MAF:
    C=0.2400/1202
    HGVS:
    NC_000018.10:g.60183864T>C, NC_000018.9:g.57851097T>C
    2.

    rs17772748 [Homo sapiens]
      AATGTACCCTGGACTTATTCATCTT[A/G]TGTTATTACTTTTTTATCTCTACAT
      Chromosome:
      18:60130586
      Validated:
      by 1000G,by cluster,by frequency,by hapmap
      Global MAF:
      G=0.0357/179
      HGVS:
      NC_000018.10:g.60130586A>G, NC_000018.9:g.57797818A>G
      3.

      rs17066582 [Homo sapiens]
        AATAACAAAAGCATAACAATGTCCT[G/T]GAAACTGTCTGTTACTATCCACACC
        Chromosome:
        18:60101295
        Validated:
        by 1000G,by cluster,by frequency,by hapmap
        Global MAF:
        G=0.0635/318
        HGVS:
        NC_000018.10:g.60101295T>G, NC_000018.9:g.57768527T>G
        4.

        rs12970134 [Homo sapiens]
          CTGACTCTTACCAAACAAAGCATGA[A/G]CAAACAAAGATTTATCAGAAGGGTG
          Chromosome:
          18:60217517
          Validated:
          by 1000G,by cluster,by frequency,by hapmap
          Global MAF:
          A=0.2075/1039
          HGVS:
          NC_000018.10:g.60217517G>A, NC_000018.9:g.57884750G>A
          5.

          rs12964203 [Homo sapiens]
            ccatattcacacctttggatcttgc[C/T]attctcagtaattgctccatttcca
            Chromosome:
            18:60236371
            Validated:
            by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
            Global MAF:
            C=0.1993/998
            HGVS:
            NC_000018.10:g.60236371T>C, NC_000018.9:g.57903604T>C
            6.

            rs12457166 [Homo sapiens]
              tgatgttccacattcactgagacca[A/G]gaggtagacaagtatctttctttct
              Chromosome:
              18:60236040
              Validated:
              by 1000G,by cluster,by frequency,by hapmap
              Global MAF:
              A=0.1278/640
              HGVS:
              NC_000018.10:g.60236040G>A, NC_000018.9:g.57903273G>A
              7.

              rs11660783 [Homo sapiens]
                ATGCTATTTTTTCTTTTTCTGACTT[C/T]TTTTATATCTCTGCTTCACTATAAG
                Chromosome:
                18:60100403
                Validated:
                by 1000G,by cluster,by frequency,by hapmap
                Global MAF:
                C=0.1000/501
                HGVS:
                NC_000018.10:g.60100403T>C, NC_000018.9:g.57767635T>C
                8.

                rs11152208 [Homo sapiens]
                  CATCAAACTATATCAAAAGTTAACA[C/T]ACCAATAAAGCTCATGGAGACCTTG
                  Chromosome:
                  18:60072566
                  Validated:
                  by 1000G,by cluster,by frequency,by hapmap
                  Global MAF:
                  C=0.1088/545
                  HGVS:
                  NC_000018.10:g.60072566T>C, NC_000018.9:g.57739798T>C
                  9.

                  rs10871777 [Homo sapiens]
                    TTGATATCTTGATGTGTTTTACACA[A/G]TGTCATGTGTGTGACTGTGCTGTTT
                    Chromosome:
                    18:60184530
                    Validated:
                    by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                    Global MAF:
                    G=0.2458/1231
                    HGVS:
                    NC_000018.10:g.60184530A>G, NC_000018.9:g.57851763A>G
                    10.

                    rs9966951 [Homo sapiens]
                      TTCTGAATTGGAATCTTATTTTTGG[A/G]CTTTGCACCCTATTCAGGAGATGTA
                      Chromosome:
                      18:60108063
                      Validated:
                      by 1000G,by cluster,by frequency,by hapmap
                      Global MAF:
                      A=0.3271/1638
                      HGVS:
                      NC_000018.10:g.60108063G>A, NC_000018.9:g.57775295G>A
                      11.

                      rs9956274 [Homo sapiens]
                        CACTTTATTCATGCATTCAAACTTA[C/T]TTGCTGCGTCCCTACTAAATGCCAA
                        Chromosome:
                        18:60245470
                        Validated:
                        by 1000G,by cluster,by frequency,by hapmap
                        Global MAF:
                        C=0.1571/787
                        HGVS:
                        NC_000018.10:g.60245470C>T, NC_000018.9:g.57912703C>T
                        12.

                        rs9954571 [Homo sapiens]
                          ACAGAGGCTGCGAAGTCCAAAATTT[A/G]TAGGACAGGCTGGTAGGCTGAAGAT
                          Chromosome:
                          18:60192644
                          Validated:
                          by 1000G,by cluster,by frequency,by hapmap
                          Global MAF:
                          A=0.1238/620
                          HGVS:
                          NC_000018.10:g.60192644G>A, NC_000018.9:g.57859877G>A
                          13.

                          rs9948303 [Homo sapiens]
                            TGGCTGAACTACATGGTGAAGAAAT[A/G]ACTAAAATGCAGATCCTCTGACTCC
                            Chromosome:
                            18:60093534
                            Validated:
                            by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                            Global MAF:
                            G=0.0803/402
                            HGVS:
                            NC_000018.10:g.60093534A>G, NC_000018.9:g.57760766A>G
                            14.

                            rs9947403 [Homo sapiens]
                              AAGTCCTTACTCCACATAAGTTTAA[A/C/T]CTCAAATCAGCTTTGTGCCTGCATG
                              Chromosome:
                              18:60202517
                              Validated:
                              by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                              Global MAF:
                              T=0.3385/1695
                              HGVS:
                              NC_000018.10:g.60202517C>A, NC_000018.10:g.60202517C>T, NC_000018.9:g.57869750C>T
                              15.

                              rs8094523 [Homo sapiens]
                                ATCAGGTGCTTTTAAAAATATTTTC[A/C/G]ATTCTCTAATCAGATGTATAAACAC
                                Chromosome:
                                18:60210922
                                Validated:
                                by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                                Global MAF:
                                A=0.0837/419
                                HGVS:
                                NC_000018.10:g.60210922G>A, NC_000018.10:g.60210922G>C, NC_000018.9:g.57878155G>A
                                16.

                                rs8085349 [Homo sapiens]
                                  CTACTAGAGGGTTGGCAGGGGTAGG[A/G]GGTTGTGCCGGGATGGGAGAATCCC
                                  Chromosome:
                                  18:60066196
                                  Validated:
                                  by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                                  Global MAF:
                                  G=0.4890/2449
                                  HGVS:
                                  NC_000018.10:g.60066196A>G, NC_000018.9:g.57733428A>G
                                  17.

                                  rs6567155 [Homo sapiens]
                                    TTTGAAAGGTCACACTTAATCTAAA[C/T]GAAATTTTCTTATATTCAAAGCACT
                                    Chromosome:
                                    18:60087885
                                    Validated:
                                    by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                                    Global MAF:
                                    T=0.3111/1558
                                    HGVS:
                                    NC_000018.10:g.60087885C>T, NC_000018.9:g.57755117C>T
                                    18.

                                    rs4940927 [Homo sapiens]
                                      TTTCAAAGAGAAAAGTAAAACTAGC[A/G/T]TAGAGTTGTTTCTCAGATCACTGGC
                                      Chromosome:
                                      18:60065457
                                      Validated:
                                      by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                                      Global MAF:
                                      A=0.3219/1612
                                      HGVS:
                                      NC_000018.10:g.60065457A>G, NC_000018.10:g.60065457A>T, NC_000018.9:g.57732689A>G
                                      19.

                                      rs4450508 [Homo sapiens]
                                        GGCAGTACTTCCTTTCTGTGGAACA[A/G]TGGCCCCAATTGGTATAGGTTATGT
                                        Chromosome:
                                        18:60246201
                                        Validated:
                                        by 1000G,by 2hit 2allele,by cluster,by frequency
                                        Global MAF:
                                        A=0.2933/1469
                                        HGVS:
                                        NC_000018.10:g.60246201G>A, NC_000018.9:g.57913434G>A
                                        20.

                                        rs3897644 [Homo sapiens]
                                          TATCTTATCAAACTTTATAGGCACT[A/G]GGGCCACAGGACAAACAATACTTCC
                                          Chromosome:
                                          18:60061837
                                          Validated:
                                          by 1000G,by 2hit 2allele,by cluster,by frequency,by hapmap
                                          Global MAF:
                                          C=0.4922/2465
                                          HGVS:
                                          NC_000018.10:g.60061837C>T, NC_000018.9:g.57729069C>T

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...
                                          Support Center