V rs655601 | |||
Location: 5:180799673 Cytogenetic region:5q35.3 Most severe consequence: Intron variant Mapped gene(s): MGAT1 Associations 1 Studies 1 |
G MGAT1 | |||
Description: alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Associations 20 Studies 19 |