rs41518645, ND6;CYTB

N. diseases: 3
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.
Optic Atrophy, Hereditary, Leber
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
46 0.925 0.200 MT 15257 missense variant G/A snv 0.700 1.000 1 1992 1992
Anemia
CUI: C0002871
Disease: Anemia
94 0.925 0.200 MT 15257 missense variant G/A snv 0.010 1.000 1 2019 2019
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.200 MT 15257 missense variant G/A snv 0.010 1.000 1 2019 2019