V rs727479 | |||
Location: 15:51242350 Cytogenetic region:15q21.2 Most severe consequence: Intron variant Mapped gene(s): CYP19A1,MIR4713HG Associations 7 Studies 7 |
G MIR4713HG | |||
Description: MIR4713 host gene Associations 193 Studies 139 |
G CYP19A1 | |||
Description: cytochrome P450 family 19 subfamily A member 1 Associations 166 Studies 115 |