V rs16879765 | |||
Location: 7:37949493 Cytogenetic region:7p14.1 Most severe consequence: Intron variant Mapped gene(s): SFRP4,EPDR1 Associations 2 Studies 2 |
G EPDR1 | |||
Description: ependymin related 1 Associations 23 Studies 18 |
G SFRP4 | |||
Description: secreted frizzled related protein 4 Associations 312 Studies 81 |