V rs17496332 | |||
Location: 1:107003753 Cytogenetic region:1p13.3 Most severe consequence: Intergenic variant Mapped gene(s): LINC01661,PRMT6 Associations 2 Studies 1 |
G LINC01661 | |||
Description: long intergenic non-protein coding RNA 1661 Associations 49 Studies 44 |
G PRMT6 | |||
Description: protein arginine methyltransferase 6 Associations 101 Studies 95 |