G INF2 | |||
Description: inverted formin 2 Associations 3 Studies 3 |
V rs56121689 | |||
Location: 14:104705145 Cytogenetic region:14q32.33 Most severe consequence: Intron variant Mapped gene(s): INF2 Associations 1 Studies 1 |
V rs72715968 | |||
Location: 14:104719841 Cytogenetic region:14q32.33 Most severe consequence: 3 prime utr variant Mapped gene(s): INF2 Associations 1 Studies 1 |
V rs4444271 | |||
Location: 14:104695125 Cytogenetic region:14q32.33 Most severe consequence: Intron variant Mapped gene(s): INF2 Associations 1 Studies 1 |