G B9D1 | |||
Description: B9 domain containing 1 Associations 13 Studies 13 |
V rs72838804 | |||
Location: 17:19338052 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): B9D1 Associations 3 Studies 3 |
V rs7221299 | |||
Location: 17:19347366 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): B9D1 Associations 1 Studies 1 |
V rs4924987 | |||
Location: 17:19343762 Cytogenetic region:17p11.2 Most severe consequence: Missense variant Mapped gene(s): B9D1 Associations 1 Studies 1 |
V rs77366811 | |||
Location: 17:19363307 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): B9D1 Associations 1 Studies 1 |
V rs9899649 | |||
Location: 17:19350300 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): B9D1 Associations 1 Studies 1 |
V rs79259362 | |||
Location: 17:19376976 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): B9D1 Associations 1 Studies 1 |
V rs1043809 | |||
Location: 17:19336119 Cytogenetic region:17p11.2 Most severe consequence: 3 prime utr variant Mapped gene(s): B9D1,EPN2 Associations 5 Studies 5 |