SLC25A22, solute carrier family 25 member 22, 79751

N. diseases: 106; N. variants: 10
Disease: Infantile encephalopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565035177
rs1565035177
Entrez Id: 79751
Gene Symbol: SLC25A22
SLC25A22
CUI: C1856408
Disease:
Infantile encephalopathy 		G 0.700 CausalMutation CLINVAR