rs150667550, NDUFS2

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.
MITOCHONDRIAL COMPLEX I DEFICIENCY
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
31 0.925 0.120 1 161210599 missense variant T/C snv 3.5E-04 1.1E-04 0.700 1.000 2 2010 2013
Leigh Disease
CUI: C0023264
Disease: Leigh Disease
114 0.925 0.120 1 161210599 missense variant T/C snv 3.5E-04 1.1E-04 0.010 1.000 1 2010 2010