Disease: Leigh Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs772294726
rs772294726
Entrez Id: 91942
Gene Symbol: NDUFAF2
NDUFAF2
CUI: C0023264
Disease:
Leigh Disease 		A 0.700 CausalMutation CLINVAR High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. 20818383 2010