SLC16A2, solute carrier family 16 member 2, 6567

N. diseases: 108; N. variants: 30
Disease: Allan-Herndon-Dudley syndrome (AHDS) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs367543059
rs367543059
Entrez Id: 6567
Gene Symbol: SLC16A2
SLC16A2
CUI: C0795889
Disease:
Allan-Herndon-Dudley syndrome (AHDS) 		C 0.700 CausalMutation CLINVAR