SLC25A22, solute carrier family 25 member 22, 79751

N. diseases: 106; N. variants: 10
Disease: Early myoclonic encephalopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797045969
rs797045969
Entrez Id: 79751
Gene Symbol: SLC25A22
SLC25A22
CUI: C0270855
Disease:
Early myoclonic encephalopathy 		A 0.700 CausalMutation CLINVAR