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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.902 118 1997 2018
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0028754
Disease: Obesity
Obesity
0.100 0.804 46 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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.100 0.842 38 1999 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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 0.813 32 2000 2014
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.100 0.960 25 2001 2018
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.100 0.789 19 2002 2019
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.846 13 2003 2018
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 0.917 12 2005 2015
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.100 0.800 10 2004 2018
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.090 1.000 9 1999 2013
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 0.778 9 2005 2013
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.090 0.778 9 2010 2014
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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 1.000 8 2008 2019
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.080 1.000 8 2008 2019
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