V rs7937 | |||
Location: 19:40796801 Cytogenetic region:19q13.2 Most severe consequence: 3 prime utr variant Mapped gene(s): RAB4B-EGLN2,MIA-RAB4B,RAB4B Associations 7 Studies 7 |
G MIA-RAB4B | |||
Description: MIA-RAB4B readthrough (NMD candidate) Associations 46 Studies 38 |
G RAB4B | |||
Description: RAB4B, member RAS oncogene family Associations 28 Studies 26 |
G RAB4B-EGLN2 | |||
Description: RAB4B-EGLN2 readthrough (NMD candidate) Associations 87 Studies 65 |