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: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.893 103 1997 2018
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0028754
Disease: Obesity
Obesity
0.100 0.837 43 1997 2018
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 0.842 38 1999 2019
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 0.813 32 2000 2019
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.100 0.955 22 2001 2014
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.100 0.778 18 2002 2013
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 1.000 12 2005 2017
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.800 10 2003 2010
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.090 1.000 9 1999 2013
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 0.778 9 2005 2013
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.080 0.875 8 2010 2014
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.070 1.000 7 2008 2015
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
Malignant neoplasm of colon and/or rectum
0.070 1.000 7 2005 2010
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.070 0.857 7 2004 2016
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.070 1.000 7 2008 2015
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.070 0.714 7 2007 2017
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.060 0.667 6 2001 2019
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.060 1.000 6 2005 2012
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.060 0.833 6 2003 2016
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.060 1.000 6 2008 2019
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.050 1.000 5 2005 2016
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.050 0.800 5 2002 2017
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 1.000 5 2001 2010
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.050 1.000 5 2001 2010
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.050 0.800 5 2002 2017