V rs7973719 | |||
Location: 12:7182217 Cytogenetic region:12p13.31 Most severe consequence: Intergenic variant Mapped gene(s): CLSTN3,PEX5 Associations 1 Studies 1 |
G CLSTN3 | |||
Description: calsyntenin 3 Associations 11 Studies 9 |
G PEX5 | |||
Description: peroxisomal biogenesis factor 5 Associations 8 Studies 7 |