V rs2949006 | |||
Location: 2:199850665 Cytogenetic region:2q33.1 Most severe consequence: Intron variant Mapped gene(s): FTCDNL1 Associations 10 Studies 10 |
G FTCDNL1 | |||
Description: formiminotransferase cyclodeaminase N-terminal like Associations 36 Studies 33 |