G CRX | |||
Description: cone-rod homeobox Associations 24 Studies 24 |
V rs10405809 | |||
Location: 19:47823958 Cytogenetic region:19q13.33 Most severe consequence: Intron variant Mapped gene(s): CRX Associations 1 Studies 1 |
V rs2879910 | |||
Location: 19:47831772 Cytogenetic region:19q13.33 Most severe consequence: Intron variant Mapped gene(s): CRX Associations 2 Studies 2 |
V rs61748438 | |||
Location: 19:47836338 Cytogenetic region:19q13.33 Most severe consequence: Missense variant Mapped gene(s): CRX Associations 2 Studies 2 |
V rs112686135 | |||
Location: 19:47838828 Cytogenetic region:19q13.33 Most severe consequence: Intron variant Mapped gene(s): CRX Associations 1 Studies 1 |
V rs563948700 | |||
Location: 19:47825763 Cytogenetic region:19q13.33 Most severe consequence: Intron variant Mapped gene(s): CRX Associations 1 Studies 1 |
V rs11668505 | |||
Location: 19:47845106 Cytogenetic region:19q13.33 Most severe consequence: Intergenic variant Mapped gene(s): CRX,TPRX2 Associations 1 Studies 1 |
V rs10410350 | |||
Location: 19:47849107 Cytogenetic region:19q13.33 Most severe consequence: Regulatory region variant Mapped gene(s): CRX,TPRX2 Associations 1 Studies 1 |
V rs62128825 | |||
Location: 19:47858980 Cytogenetic region:19q13.33 Most severe consequence: Intergenic variant Mapped gene(s): CRX,TPRX2 Associations 3 Studies 3 |
V rs76531193 | |||
Location: 19:47857434 Cytogenetic region:19q13.33 Most severe consequence: Intergenic variant Mapped gene(s): CRX,TPRX2 Associations 9 Studies 9 |
V rs62128824 | |||
Location: 19:47858667 Cytogenetic region:19q13.33 Most severe consequence: Intergenic variant Mapped gene(s): CRX,TPRX2 Associations 2 Studies 2 |
V rs7252257 | |||
Location: 19:47852721 Cytogenetic region:19q13.33 Most severe consequence: Intergenic variant Mapped gene(s): CRX,TPRX2 Associations 1 Studies 1 |
T level of cone-rod homeobox protein in blood OBA_2051331 | |||
The amount of a cone-rod homeobox protein when measured in blood. Associations 0 Studies 2 |