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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Breast Carcinoma
|
2793 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.030 | 1.000 | 3 | 2011 | 2019 | ||||||
Chronic Obstructive Airway Disease
|
852 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.030 | 0.333 | 3 | 2004 | 2017 | ||||||
Malignant neoplasm of breast
|
3417 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.030 | 1.000 | 3 | 2011 | 2019 | ||||||
Neoplasms
|
1644 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.030 | 1.000 | 3 | 2011 | 2018 | ||||||
Asthma
|
1536 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2009 | 2010 | ||||||
Carcinoma of lung
|
1204 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2016 | 2019 | ||||||
Coronary heart disease
|
1178 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2012 | 2019 | ||||||
Cystic Fibrosis
|
704 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2007 | 2008 | ||||||
Malignant neoplasm of lung
|
1142 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2016 | 2019 | ||||||
Non-Small Cell Lung Carcinoma
|
712 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2009 | 2013 | ||||||
Pneumonitis
|
13 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2009 | 2016 | ||||||
Primary malignant neoplasm of lung
|
981 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.020 | 1.000 | 2 | 2016 | 2019 | ||||||
Adult Glioblastoma
|
98 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Bone Diseases
|
10 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
Childhood Glioblastoma
|
98 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Congenital heart disease
|
80 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Degenerative polyarthritis
|
247 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
Glioblastoma
|
281 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Glioblastoma Multiforme
|
186 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Hepatitis C
|
347 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Hypertensive disease
|
1085 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
Myocardial Infarction
|
680 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||
Obesity
|
1111 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
Osteoarthritis, Knee
|
150 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
Osteoporotic Fractures
|
40 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2016 | 2016 |