V GPHN | |||
This variant could not be mapped to the genome. Associations 1 Studies 1 |
G GPHN | |||
Description: gephyrin Associations 18 Studies 18 |
V rs8020095 | |||
Location: 14:66987141 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs146647518 | |||
Location: 14:67062903 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs72728697 | |||
Location: 14:66886390 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs17103572 | |||
Location: 14:66519254 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs6573725 | |||
Location: 14:66857742 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs6573723 | |||
Location: 14:66769004 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs113330417 | |||
Location: 14:66782703 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs190850598 | |||
Location: 14:66645703 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs7151773 | |||
Location: 14:66557282 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs554687762 | |||
Location: 14:66530663 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs7146638 | |||
Location: 14:67146675 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs79421291 | |||
Location: 14:67133673 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs72724601 | |||
Location: 14:66587466 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs139629302 | |||
Location: 14:66632778 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs149283784 | |||
Location: 14:66813548 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs75469396 | |||
Location: 14:66627835 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs112579020 | |||
Location: 14:66662340 Cytogenetic region:14q23.3 Most severe consequence: Intron variant Mapped gene(s): GPHN Associations 1 Studies 1 |
V rs555218597 | |||
Location: 14:67187837 Cytogenetic region:14q23.3 Most severe consequence: Regulatory region variant Mapped gene(s): GPHN,GARIN2 Associations 1 Studies 1 |