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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 97909892 | intron variant | A/G | snv | 0.23 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 2 | 2014 | 2019 | |||||||||
|
1 | 97934347 | intron variant | G/T | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 97388977 | intron variant | C/A | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 97850337 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
1 | 97221459 | intron variant | C/T | snv | 0.41 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1 | 97221459 | intron variant | C/T | snv | 0.41 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1 | 97743554 | intron variant | T/C | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 97450059 | missense variant | G/A;C | snv | 4.2E-04; 1.6E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1 | 97450059 | missense variant | G/A;C | snv | 4.2E-04; 1.6E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1 | 97207282 | intron variant | T/C | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1 | 97856823 | non coding transcript exon variant | C/T | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 97573863 | synonymous variant | C/T | snv | 1.4E-02 | 1.3E-02 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1 | 97183653 | intron variant | G/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1 | 97412887 | intron variant | C/A | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 97181782 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1 | 97691775 | missense variant | C/T | snv | 1.2E-05 |
|
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
1 | 97861577 | intron variant | A/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 97861577 | intron variant | A/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 97864883 | intron variant | T/C | snv | 7.0E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 97823025 | intron variant | T/C;G | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 97957593 | intron variant | G/A | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.020 | 1.000 | 2 | 2016 | 2017 | |||||||
|
0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 |