G EMC2 | |||
Description: ER membrane protein complex subunit 2 Associations 27 Studies 27 |
V rs79593277 | |||
Location: 8:108483382 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 2 Studies 2 |
V rs182955453 | |||
Location: 8:108471735 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 1 Studies 1 |
V rs4734176 | |||
Location: 8:108447103 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 1 Studies 1 |
V rs150271015 | |||
Location: 8:108463946 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 1 Studies 1 |
V rs1789961 | |||
Location: 8:108466268 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 1 Studies 1 |
V rs79437808 | |||
Location: 8:108585572 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 2 Studies 2 |
V rs77442195 (rs766047297) | |||
Location: 8:108467508 Cytogenetic region:8q23.1 Most severe consequence: Intron variant Mapped gene(s): EMC2 Associations 1 Studies 1 |
V rs1580347 | |||
Location: 8:108520009 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs9297415 | |||
Location: 8:108560331 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs16878149 | |||
Location: 8:108557470 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs4735071 | |||
Location: 8:108563606 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs10089785 | |||
Location: 8:108587740 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 3 Studies 3 |
V rs5893926 | |||
Location: 8:108537508 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 2 Studies 2 |
V rs1480560 | |||
Location: 8:108560622 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs1789964 | |||
Location: 8:108514499 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs11787476 | |||
Location: 8:108521662 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs62537502 | |||
Location: 8:108527762 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs192498131 | |||
Location: 8:108537032 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 2 Studies 2 |
V rs7813717 | |||
Location: 8:108534556 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs6990000 | |||
Location: 8:108576011 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |
V rs10808424 (rs61235542) | |||
Location: 8:108507494 Cytogenetic region:8q23.1 Most severe consequence: Intergenic variant Mapped gene(s): TMEM74,EMC2 Associations 1 Studies 1 |