Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs908832
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.030 1.000 3 2005 2013
dbSNP: rs770030911
rs770030911
ABCA2
1.000 0.080 9 137016400 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2013 2013
dbSNP: rs908832
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 < 0.001 1 2006 2006
dbSNP: rs908832
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 < 0.001 1 2006 2006
dbSNP: rs908832
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 < 0.001 1 2006 2006