V rs888219 | |||
Location: 9:126166744 Cytogenetic region:9q33.3 Most severe consequence: Intergenic variant Mapped gene(s): PBX3,MVB12B Associations 1 Studies 1 |
G PBX3 | |||
Description: PBX homeobox 3 Associations 58 Studies 55 |
G MVB12B | |||
Description: multivesicular body subunit 12B Associations 72 Studies 66 |