C2, complement C2, 717

N. diseases: 71; N. variants: 39
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: rs685031
rs685031 		1.000 0.040 6 31913954 intron variant G/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs3130683
rs3130683 		1.000 0.040 6 31920590 intron variant C/T snv 0.91
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs644045
rs644045 		0.851 0.240 6 31916180 intron variant A/G snv 0.72
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018