Location: 11:2915722 Cytogenetic region:11p15.4 Most severe consequence: Intron variant Mapped gene(s): SLC22A18
Associations 7 Studies 7
Description: solute carrier family 22 member 18Location: 11:2899721-2925246 Cytogenetic region: 11p15.4 Biotype: protein coding
Associations 29 Studies 29