Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606891
rs267606891
Entrez Id: 4514;4537;4538;4539
Gene Symbol: COX3;ND3;ND4;ND4L
COX3;ND3;ND4;ND4L
CUI: C1839040
Disease:
LEBER OPTIC ATROPHY AND DYSTONIA
A 0.700 CausalMutation CLINVAR