rs387906780, SDHA

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.
PARAGANGLIOMAS 5
CUI: C3279992
Disease: PARAGANGLIOMAS 5
39 0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05 0.800 1.000 8 2010 2017
Mitochondrial Complex II Deficiency
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
45 0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05 0.700 1.000 7 2010 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05 0.700 1.000 7 2009 2014
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
36 0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05 0.010 1.000 1 2010 2010