SLC25A13, solute carrier family 25 member 13, 10165

N. diseases: 109; N. variants: 23
Disease: Citrin deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338726
rs80338726
Entrez Id: 10165
Gene Symbol: SLC25A13
SLC25A13
CUI: C1997910
Disease:
Citrin deficiency 		GT 0.700 CausalMutation CLINVAR