Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 7 | 141972905 | missense variant | G/A | snv | 0.50 | 0.47 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.925 | 0.120 | 7 | 141972905 | missense variant | G/A | snv | 0.50 | 0.47 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.925 | 0.120 | 7 | 141972905 | missense variant | G/A | snv | 0.50 | 0.47 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
7 | 141972869 | missense variant | C/T | snv | 1.6E-04 | 1.7E-04 |
|
Neoplasms | 0.010 | 1.000 | 1 | 1995 | 1995 | ||||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.851 | 0.160 | 7 | 141973545 | missense variant | C/G | snv | 0.46 | 0.44 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
7 | 141973254 | missense variant | C/A | snv | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 |