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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 46765770 | intron variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 17 | 46770468 | intron variant | T/A;G | snv |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 17 | 46770468 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 17 | 46770468 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 17 | 46770948 | intron variant | G/T | snv | 0.25 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.120 | 17 | 46773719 | missense variant | A/C;G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 0 | |||||||||||
|
17 | 46776506 | intron variant | G/A | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.120 | 17 | 46779275 | intron variant | G/C | snv | 0.84 |
|
Nervous System Diseases | 0.800 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.120 | 17 | 46779275 | intron variant | G/C | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 46779275 | intron variant | G/C | snv | 0.84 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 17 | 46779515 | intron variant | G/A | snv | 0.84 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 17 | 46779515 | intron variant | G/A | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
17 | 46779986 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
17 | 46781362 | intron variant | G/A | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
17 | 46781489 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
17 | 46781665 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1.000 | 0.040 | 17 | 46781778 | intron variant | C/T | snv | 0.84 |
|
Nervous System Diseases | 0.800 | 1.000 | 2 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 17 | 46781778 | intron variant | C/T | snv | 0.84 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 17 | 46781778 | intron variant | C/T | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 46782044 | intron variant | A/G | snv | 0.84 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.120 | 17 | 46782044 | intron variant | A/G | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 46782044 | intron variant | A/G | snv | 0.84 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.120 | 17 | 46782044 | intron variant | A/G | snv | 0.84 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 17 | 46782349 | intron variant | T/C | snv | 0.84 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 17 | 46782349 | intron variant | T/C | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |