Location: 17:81261988 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): SLC38A10
Associations 1 Studies 1
Description: solute carrier family 38 member 10Location: 17:81244811-81295547 Cytogenetic region: 17q25.3 Biotype: protein coding
Associations 12 Studies 8