Disease | N. SNPs d | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AFEXOME | AFGENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Diabetes Mellitus, Non-Insulin-Dependent
|
2672 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.900 | 0.902 | 122 | 1997 | 2018 | ||||
Obesity
|
1111 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.804 | 46 | 1997 | 2018 | ||||
Diabetes Mellitus
|
824 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.842 | 38 | 1999 | 2018 | ||||
Diabetes
|
710 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.813 | 32 | 2000 | 2014 | ||||
Metabolic Syndrome X
|
591 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.960 | 25 | 2001 | 2018 | ||||
Polycystic Ovary Syndrome
|
363 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.789 | 19 | 2002 | 2019 | ||||
Colorectal Carcinoma
|
1962 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.846 | 13 | 2003 | 2018 | ||||
Coronary Artery Disease
|
1577 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.917 | 12 | 2005 | 2015 | ||||
Gestational Diabetes
|
224 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.100 | 0.800 | 10 | 2004 | 2018 | ||||
Coronary heart disease
|
1178 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.090 | 0.778 | 9 | 2005 | 2013 | ||||
Hyperinsulinism
|
64 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.090 | 1.000 | 9 | 1999 | 2013 | ||||
Non-alcoholic Fatty Liver Disease
|
222 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.090 | 0.778 | 9 | 2010 | 2014 | ||||
Malignant neoplasm of stomach
|
615 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.080 | 1.000 | 8 | 2008 | 2019 | ||||
Stomach Carcinoma
|
652 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.080 | 1.000 | 8 | 2008 | 2019 | ||||
Breast Carcinoma
|
2793 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 0.857 | 7 | 2002 | 2018 | ||||
Hypertensive disease
|
1085 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 0.714 | 7 | 2001 | 2019 | ||||
Malignant neoplasm of breast
|
3417 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 0.857 | 7 | 2002 | 2018 | ||||
Malignant neoplasm of colon and/or rectum
|
502 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 1.000 | 7 | 2005 | 2010 | ||||
Malignant Neoplasms
|
1641 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 1.000 | 7 | 2001 | 2014 | ||||
Primary malignant neoplasm
|
1374 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.070 | 1.000 | 7 | 2001 | 2014 | ||||
Alzheimer's Disease
|
1843 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.060 | 0.500 | 6 | 2005 | 2015 | ||||
Cardiovascular Diseases
|
711 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.060 | 0.833 | 6 | 2003 | 2015 | ||||
Coronary Arteriosclerosis
|
440 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.060 | 1.000 | 6 | 2005 | 2012 | ||||
Diabetic Nephropathy
|
238 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.060 | 0.667 | 6 | 2007 | 2012 | ||||
Impaired cognition
|
348 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 0.060 | 1.000 | 6 | 2008 | 2019 |