SLC6A8, solute carrier family 6 member 8, 6535

N. diseases: 274; N. variants: 27
Disease: Creatine deficiency, X-linked ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569539466
rs1569539466
Entrez Id: 6535
Gene Symbol: SLC6A8
SLC6A8
CUI: C1845862
Disease:
Creatine deficiency, X-linked 		G 0.700 CausalMutation CLINVAR