C5, complement C5, 727

N. diseases: 129; N. variants: 20
Disease: Coronary Artery Disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs41311933
rs41311933 		1.000 0.040 9 120977282 intron variant C/T snv 6.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018