Source: ALL

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: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 0.974 39 1998 2020
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.100 0.895 19 2002 2020
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 0.849 53 1998 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.100 0.917 36 1998 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 0.917 24 1998 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.100 1.000 20 2005 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.944 18 2000 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction
0.100 1.000 13 2003 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.060 0.833 6 2005 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.060 0.833 6 2004 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 0.750 4 2014 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 0.750 4 2014 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C3647902
Disease: Vasculogenic erectile dysfunction
Vasculogenic erectile dysfunction
0.030 1.000 3 2011 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
Secondary malignant neoplasm of lymph node
0.010 < 0.001 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure
0.010 1.000 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.010 1.000 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis
0.010 1.000 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.010 < 0.001 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.010 1.000 1 2019 2019
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.100 1.000 15 2004 2018
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 0.933 15 2006 2018
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.100 0.818 11 1999 2018
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.100 0.818 11 1999 2018