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: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2019 2019
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2019 2019
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2012 2012
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2015 2015
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		0.010 < 0.001 1 2011 2011
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2015 2015
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2019 2019
dbSNP: rs146292819
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2015 2015