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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hereditary hemochromatosis
|
56 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.991 | 114 | 1996 | 2019 | ||||
HEMOCHROMATOSIS, TYPE 1
|
62 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.960 | 99 | 1996 | 2019 | ||||
Iron Overload
|
53 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.886 | 79 | 1997 | 2019 | ||||
Hemochromatosis
|
45 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.961 | 77 | 1997 | 2019 | ||||
Alzheimer's Disease
|
1843 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.882 | 17 | 2003 | 2016 | ||||
Hepatitis C
|
347 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.929 | 14 | 2000 | 2010 | ||||
Diabetes Mellitus, Non-Insulin-Dependent
|
2672 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.833 | 12 | 2001 | 2016 | ||||
Liver carcinoma
|
942 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.917 | 12 | 2000 | 2015 | ||||
Amyotrophic Lateral Sclerosis
|
485 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.636 | 11 | 2007 | 2016 | ||||
Liver Cirrhosis
|
189 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.909 | 11 | 2001 | 2017 | ||||
Liver diseases
|
100 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.818 | 11 | 1999 | 2011 | ||||
Porphyria Cutanea Tarda
|
39 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 0.909 | 11 | 1998 | 2014 | ||||
Neurodegenerative Disorders
|
85 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.100 | 1.000 | 10 | 2006 | 2018 | ||||
Cirrhosis
|
110 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.090 | 0.889 | 9 | 2001 | 2011 | ||||
Breast Carcinoma
|
2793 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.080 | 0.875 | 8 | 2006 | 2015 | ||||
Diabetes Mellitus
|
824 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.080 | 0.875 | 8 | 2000 | 2018 | ||||
Hepatitis C, Chronic
|
80 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.080 | 0.875 | 8 | 1999 | 2010 | ||||
Malignant neoplasm of breast
|
3417 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.080 | 0.875 | 8 | 2006 | 2015 | ||||
Diabetes
|
710 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.070 | 0.857 | 7 | 2000 | 2018 | ||||
Hypocalciuric hypercalcemia, familial, type 1
|
58 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.070 | 1.000 | 7 | 1999 | 2002 | ||||
Diastolic blood pressure
|
1037 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 6 | 2011 | 2018 | ||||
Coronary heart disease
|
1178 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.060 | 1.000 | 6 | 1998 | 2013 | ||||
Malignant Neoplasms
|
1641 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.060 | 1.000 | 6 | 2004 | 2016 | ||||
Primary malignant neoplasm
|
1374 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.060 | 1.000 | 6 | 2004 | 2016 | ||||
Steatohepatitis
|
75 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.060 | 0.833 | 6 | 2006 | 2012 |