V rs934299 | |||
Location: 2:136581370 Cytogenetic region:2q22.1 Most severe consequence: Intergenic variant Mapped gene(s): THSD7B,SMC4P1 Associations 1 Studies 1 |
G SMC4P1 | |||
Description: structural maintenance of chromosomes 4 pseudogene 1 Associations 47 Studies 41 |
G THSD7B | |||
Description: thrombospondin type 1 domain containing 7B Associations 142 Studies 105 |