U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 405

1.

rs1490133996 [Homo sapiens]
    Variant type:
    SNV:
    Alleles:
    G>A,C
    Chromosome:
    no mapping
    Canonical SPDI:

    2.

    rs1488246290 [Homo sapiens]
      Variant type:
      SNV:
      Alleles:
      A>T
      Chromosome:
      no mapping
      Canonical SPDI:

      3.

      rs1488149227 [Homo sapiens]
        Variant type:
        SNV:
        Alleles:
        T>C
        Chromosome:
        no mapping
        Canonical SPDI:

        4.

        rs1486616351 [Homo sapiens]
          Variant type:
          SNV:
          Alleles:
          A>G
          Chromosome:
          no mapping
          Canonical SPDI:

          5.

          rs1485826587 [Homo sapiens]
            Variant type:
            SNV:
            Alleles:
            G>T
            Chromosome:
            no mapping
            Canonical SPDI:

            6.

            rs1484710420 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              C>T
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1483238284 [Homo sapiens]
                Variant type:
                SNV:
                Alleles:
                A>T
                Chromosome:
                no mapping
                Canonical SPDI:

                8.

                rs1481570020 [Homo sapiens]
                  Variant type:
                  SNV:
                  Alleles:
                  T>A
                  Chromosome:
                  no mapping
                  Canonical SPDI:

                  9.

                  rs1480843528 [Homo sapiens]
                    Variant type:
                    SNV:
                    Alleles:
                    G>A
                    Chromosome:
                    no mapping
                    Canonical SPDI:

                    10.

                    rs1479936544 [Homo sapiens]
                      Variant type:
                      SNV:
                      Alleles:
                      C>T
                      Chromosome:
                      no mapping
                      Canonical SPDI:

                      11.

                      rs1477243492 [Homo sapiens]
                        Variant type:
                        SNV:
                        Alleles:
                        ->T
                        Chromosome:
                        no mapping
                        Canonical SPDI:

                        12.

                        rs1473837591 [Homo sapiens]
                          Variant type:
                          SNV:
                          Alleles:
                          G>T
                          Chromosome:
                          no mapping
                          Canonical SPDI:

                          13.

                          rs1471641169 [Homo sapiens]
                            Variant type:
                            SNV:
                            Alleles:
                            CTACCACAGGC>-
                            Chromosome:
                            no mapping
                            Canonical SPDI:

                            14.

                            rs1470999904 [Homo sapiens]
                              Variant type:
                              SNV:
                              Alleles:
                              C>T
                              Chromosome:
                              no mapping
                              Canonical SPDI:

                              15.

                              rs1469870667 [Homo sapiens]
                                Variant type:
                                SNV:
                                Alleles:
                                A>G
                                Chromosome:
                                no mapping
                                Canonical SPDI:

                                16.

                                rs1469860136 [Homo sapiens]
                                  Variant type:
                                  SNV:
                                  Alleles:
                                  G>A
                                  Chromosome:
                                  no mapping
                                  Canonical SPDI:

                                  17.

                                  rs1468865353 [Homo sapiens]
                                    Variant type:
                                    SNV:
                                    Alleles:
                                    T>G
                                    Chromosome:
                                    no mapping
                                    Canonical SPDI:

                                    18.

                                    rs1465869018 [Homo sapiens]
                                      Variant type:
                                      SNV:
                                      Alleles:
                                      G>A,T
                                      Chromosome:
                                      no mapping
                                      Canonical SPDI:

                                      19.

                                      rs1465540483 [Homo sapiens]
                                        Variant type:
                                        SNV:
                                        Alleles:
                                        C>A
                                        Chromosome:
                                        no mapping
                                        Canonical SPDI:

                                        20.

                                        rs1462117124 [Homo sapiens]
                                          Variant type:
                                          SNV:
                                          Alleles:
                                          T>C
                                          Chromosome:
                                          no mapping
                                          Canonical SPDI:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...