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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.120 | 1 | 201899905 | stop gained | G/A;C | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 |
|
0.700 | 1.000 | 2 | 2017 | 2017 | ||||||||
|
1 | 201900129 | missense variant | G/A | snv | 0.28 | 0.28 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.040 | 1 | 201917642 | intron variant | A/- | delins | 0.25 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 |
|
Cardiovascular Diseases | 0.710 | 1.000 | 2 | 2017 | 2018 | |||||||
|
1.000 | 0.040 | 1 | 201917642 | intron variant | A/- | delins | 0.25 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 201901093 | intron variant | A/G | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.882 | 0.120 | 1 | 201899905 | stop gained | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1 | 201941435 | intron variant | C/T | snv | 0.98 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 201946530 | 5 prime UTR variant | A/C | snv | 0.92 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 201939550 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1 | 201943694 | intron variant | G/A | snv | 0.96 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 1 | 201918593 | intron variant | T/C | snv | 0.32 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.882 | 0.120 | 1 | 201899905 | stop gained | G/A;C | snv |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 1 | 201918593 | intron variant | T/C | snv | 0.32 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1 | 201941435 | intron variant | C/T | snv | 0.98 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 201946530 | 5 prime UTR variant | A/C | snv | 0.92 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 201939550 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1 | 201943694 | intron variant | G/A | snv | 0.96 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.882 | 0.120 | 1 | 201899905 | stop gained | G/A;C | snv |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 |