G NOX5 | |||
Description: NADPH oxidase 5 Associations 9 Studies 6 |
G SPESP1-NOX5 | |||
Description: SPESP1-NOX5 readthrough Associations 10 Studies 7 |
V rs311904 | |||
Location: 15:69054606 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 2 Studies 1 |
V rs148060387 | |||
Location: 15:69037050 Cytogenetic region:15q23 Most severe consequence: Missense variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs4776428 | |||
Location: 15:69052059 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs12443247 | |||
Location: 15:69024929 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs311893 | |||
Location: 15:69033241 Cytogenetic region:15q23 Most severe consequence: Missense variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs147193228 | |||
Location: 15:69029618 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs77425808 | |||
Location: 15:69051985 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs139560487 | |||
Location: 15:69052764 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5,NOX5 Associations 1 Studies 1 |
V rs10851796 | |||
Location: 15:68999161 Cytogenetic region:15q23 Most severe consequence: Intron variant Mapped gene(s): SPESP1-NOX5 Associations 1 Studies 1 |