rs387906900, OPA1

N. diseases: 2
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 WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
22 0.925 0.160 3 193643978 missense variant G/T snv 0.800 1.000 8 2004 2013
Optic Atrophy 1
CUI: C0338508
Disease: Optic Atrophy 1
45 0.925 0.160 3 193643978 missense variant G/T snv 0.700 1.000 20 2000 2013