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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
20 | 37698121 | intron variant | A/G | snv | 9.3E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | 0.080 | 20 | 37754119 | intron variant | C/T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.080 | 20 | 37754119 | intron variant | C/T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.080 | 20 | 37754119 | intron variant | C/T | snv | 0.12 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
20 | 37841292 | intron variant | G/A | snv | 0.81 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||||
|
20 | 37841292 | intron variant | G/A | snv | 0.81 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||||
|
0.882 | 0.160 | 20 | 37771178 | intron variant | G/T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.882 | 0.160 | 20 | 37771178 | intron variant | G/T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.882 | 0.160 | 20 | 37771178 | intron variant | G/T | snv | 0.12 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
20 | 37710922 | intron variant | G/C | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | 0.080 | 20 | 37758210 | intron variant | G/A | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.080 | 20 | 37758210 | intron variant | G/A | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 20 | 37758210 | intron variant | G/A | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.080 | 20 | 37758210 | intron variant | G/A | snv | 0.12 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
20 | 37843596 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||||
|
0.882 | 0.160 | 20 | 37771178 | intron variant | G/T | snv | 0.12 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.020 | 1.000 | 2 | 2008 | 2009 | |||||||
|
1.000 | 0.080 | 20 | 37733022 | missense variant | G/A;C | snv | 8.0E-06; 8.0E-06 |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.160 | 20 | 37771178 | intron variant | G/T | snv | 0.12 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.080 | 20 | 37777265 | intron variant | A/G | snv | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.080 | 20 | 37777265 | intron variant | A/G | snv | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 |