SLC16A2, solute carrier family 16 member 2, 6567

N. diseases: 108; N. variants: 30
Disease: Mental Retardation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs122455132
rs122455132
Entrez Id: 6567
Gene Symbol: SLC16A2
SLC16A2
CUI: C0025362
Disease:
Mental Retardation 		C 0.700 CausalMutation CLINVAR