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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 6 | 160100853 | intron variant | C/T | snv | 5.0E-02 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 6 | 160100853 | intron variant | C/T | snv | 5.0E-02 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
6 | 160085430 | intron variant | G/A | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160077017 | intron variant | G/A | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.120 | 6 | 159990235 | intron variant | A/G | snv | 0.83 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 6 | 159990235 | intron variant | A/G | snv | 0.83 |
|
Digestive System Diseases; Neoplasms | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 6 | 160044259 | intron variant | G/A | snv | 0.57 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
6 | 159974255 | intron variant | TTCTT/-;TTCTTTTCTT | delins | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
6 | 160075211 | intron variant | T/G | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
6 | 159990715 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 6 | 160082624 | intron variant | C/T | snv | 0.15 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.882 | 0.040 | 6 | 160047351 | intron variant | T/A;C | snv | 0.53 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.040 | 6 | 160047351 | intron variant | T/A;C | snv | 0.53 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.040 | 6 | 160047351 | intron variant | T/A;C | snv | 0.53 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
6 | 160096856 | intron variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
0.700 | 1.000 | 2 | 2018 | 2018 | |||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 |
|
Digestive System Diseases; Neoplasms | 0.010 | < 0.001 | 1 | 2019 | 2019 | ||||||
|
0.925 | 0.080 | 6 | 160027292 | missense variant | C/G | snv | 0.13 | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 |