rs9809219, SDHA

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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.925 0.120 5 251100 missense variant C/T snv 4.0E-05 1.4E-05 0.700 1.000 10 1995 2017
Leigh Disease
CUI: C0023264
Disease: Leigh Disease
114 0.925 0.120 5 251100 missense variant C/T snv 4.0E-05 1.4E-05 0.700 0
Mitochondrial Complex II Deficiency
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
45 0.925 0.120 5 251100 missense variant C/T snv 4.0E-05 1.4E-05 0.700 0