rs397515508, ND2;ND1

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Abnormal vision
CUI: C3665386
Disease: Abnormal vision
6 0.925 0.160 MT 3700 missense variant G/A snv 0.700 0
Electroretinogram abnormal
CUI: C0476397
Disease: Electroretinogram abnormal
10 0.925 0.160 MT 3700 missense variant G/A snv 0.700 0
Optic Atrophy, Hereditary, Leber
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
46 0.925 0.160 MT 3700 missense variant G/A snv 0.700 0
Optic Neuropathy
CUI: C3887709
Disease: Optic Neuropathy
8 0.925 0.160 MT 3700 missense variant G/A snv 0.700 0