rs770966290, OPA1

N. diseases: 2
Disease: Dominant hereditary optic atrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dominant hereditary optic atrophy
CUI: C4551508
Disease: Dominant hereditary optic atrophy
0.010 GeneticVariation BEFREE Thus, a pronounced decline with age in GC-IPL thickness is observed in c.2708_2711delTTAG ADOA, an intermediate decline with age is observed in c.983A>G ADOA, whereas little or no change with age is observed in c.2826_2836delinsGGATGCTCCA ADOA. 26385429 2015