V NOD2 | |||
This variant could not be mapped to the genome. Associations 1 Studies 1 |
G NOD2 | |||
Description: nucleotide binding oligomerization domain containing 2 Associations 46 Studies 44 |
V rs5743289 | |||
Location: 16:50722863 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 5 Studies 5 |
V rs2076756 | |||
Location: 16:50722970 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 9 Studies 9 |
V rs17221417 | |||
Location: 16:50705671 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 2 Studies 2 |
V rs2066844 | |||
Location: 16:50712015 Cytogenetic region:16q12.1 Most severe consequence: Missense variant Mapped gene(s): NOD2 Associations 10 Studies 10 |
V rs6500328 | |||
Location: 16:50702745 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs2066845 | |||
Location: 16:50722629 Cytogenetic region:16q12.1 Most severe consequence: Missense variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs142997491 | |||
Location: 16:50695909 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs34133110 | |||
Location: 16:50710008 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs74477363 | |||
Location: 16:50694107 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs145293873 | |||
Location: 16:50711028 Cytogenetic region:16q12.1 Most severe consequence: Missense variant Mapped gene(s): NOD2 Associations 1 Studies 1 |
V rs9302752 | |||
Location: 16:50685192 Cytogenetic region:16q12.1 Most severe consequence: Regulatory region variant Mapped gene(s): NOD2,SNX20 Associations 3 Studies 3 |
V rs7194886 | |||
Location: 16:50691282 Cytogenetic region:16q12.1 Most severe consequence: Intergenic variant Mapped gene(s): NOD2,SNX20 Associations 1 Studies 1 |
V rs1420685 | |||
Location: 16:50685763 Cytogenetic region:16q12.1 Most severe consequence: Intergenic variant Mapped gene(s): NOD2,SNX20 Associations 1 Studies 1 |
V rs113593463 | |||
Location: 16:50685832 Cytogenetic region:16q12.1 Most severe consequence: Regulatory region variant Mapped gene(s): NOD2,SNX20 Associations 1 Studies 1 |
V rs2066847 | |||
Location: 16:50729868 Cytogenetic region:16q12.1 Most severe consequence: Frameshift variant Mapped gene(s): CYLD-AS1,NOD2 Associations 6 Studies 6 |
V rs2066847 (rs5743293) | |||
Location: 16:50729868 Cytogenetic region:16q12.1 Most severe consequence: Frameshift variant Mapped gene(s): CYLD-AS1,NOD2 Associations 1 Studies 1 |
V rs72796367 | |||
Location: 16:50728860 Cytogenetic region:16q12.1 Most severe consequence: Intron variant Mapped gene(s): CYLD-AS1,NOD2 Associations 1 Studies 1 |