G FLCN | |||
Description: folliculin Associations 9 Studies 8 |
V rs10459910 | |||
Location: 17:17233577 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs1736213 | |||
Location: 17:17231214 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs35488709 | |||
Location: 17:17222040 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs8080386 | |||
Location: 17:17218310 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs1736221 | |||
Location: 17:17222281 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs1736220 | |||
Location: 17:17223478 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN Associations 1 Studies 1 |
V rs12600635 | |||
Location: 17:17239582 Cytogenetic region:17p11.2 Most severe consequence: Intergenic variant Mapped gene(s): ACTG1P24,FLCN Associations 2 Studies 1 |
V rs4985752 | |||
Location: 17:17217498 Cytogenetic region:17p11.2 Most severe consequence: Intron variant Mapped gene(s): FLCN,MPRIP Associations 1 Studies 1 |