G CLCN5 | |||
Description: chloride voltage-gated channel 5 Associations 5 Studies 5 |
V rs188104254 | |||
Location: X:49930986 Cytogenetic region:Xp11.23 Most severe consequence: Intron variant Mapped gene(s): CLCN5 Associations 1 Studies 1 |
V rs782567961 | |||
Location: X:49950463 Cytogenetic region:Xp11.23 Most severe consequence: Intron variant Mapped gene(s): CLCN5 Associations 1 Studies 1 |
V rs147570790 | |||
Location: X:50072966 Cytogenetic region:Xp11.23 Most severe consequence: Intron variant Mapped gene(s): CLCN5 Associations 1 Studies 1 |
V rs232758 | |||
Location: X:49962327 Cytogenetic region:Xp11.23 Most severe consequence: Intron variant Mapped gene(s): CLCN5 Associations 1 Studies 1 |
V rs113957181 | |||
Location: X:50083943 Cytogenetic region:Xp11.23 Most severe consequence: Intron variant Mapped gene(s): CLCN5 Associations 1 Studies 1 |