Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356530
rs80356530
OPA1 ; LOC102724808
C 0.700 CausalMutation CLINVAR Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy. 11440989

2001