G NR4A3 | |||
Description: nuclear receptor subfamily 4 group A member 3 Associations 7 Studies 6 |
V rs191205566 | |||
Location: 9:99824951 Cytogenetic region:9q31.1 Most severe consequence: Intron variant Mapped gene(s): NR4A3,NAMA Associations 1 Studies 1 |
V rs7023690 | |||
Location: 9:99861046 Cytogenetic region:9q31.1 Most severe consequence: Intron variant Mapped gene(s): NR4A3,NAMA Associations 2 Studies 2 |
V rs1405209 | |||
Location: 9:99823263 Cytogenetic region:9q31.1 Most severe consequence: Intron variant Mapped gene(s): NR4A3,NAMA Associations 3 Studies 2 |
V rs34711370 (rs147117699) | |||
Location: 9:99865302 Cytogenetic region:9q31.1 Most severe consequence: 3 prime utr variant Mapped gene(s): NR4A3,NAMA Associations 1 Studies 1 |