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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 3 | 66173478 | intron variant | G/A | snv | 0.13 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.080 | 3 | 66173478 | intron variant | G/A | snv | 0.13 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 3 | 66221128 | splice donor variant | G/A | snv | 7.6E-06 | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 3 | 66262055 | missense variant | C/T | snv | 7.0E-06 |
|
0.800 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 3 | 66263369 | missense variant | T/G | snv |
|
0.800 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 66314739 | intron variant | G/A | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 3 | 66361431 | intron variant | T/C | snv | 0.55 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 3 | 66361431 | intron variant | T/C | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 3 | 66361431 | intron variant | T/C | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 3 | 66369505 | missense variant | C/T | snv |
|
0.800 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
3 | 66376835 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
3 | 66381178 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
3 | 66381178 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
1.000 | 0.040 | 3 | 66383098 | missense variant | G/A;C | snv | 1.4E-04; 4.0E-06 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 3 | 66383098 | missense variant | G/A;C | snv | 1.4E-04; 4.0E-06 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 3 | 66383098 | missense variant | G/A;C | snv | 1.4E-04; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2018 | 2018 |