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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 112970444 | intron variant | A/G | snv | 4.2E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
10 | 112970444 | intron variant | A/G | snv | 4.2E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
10 | 112961478 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
10 | 113153211 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 113144442 | intron variant | T/G | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 113146078 | missense variant | G/A | snv | 4.0E-06 | 7.1E-06 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
10 | 112955839 | intron variant | G/A | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 112995025 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 112995025 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 113087161 | intron variant | T/C | snv | 1.3E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
10 | 113035497 | intron variant | G/C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
10 | 113005988 | intron variant | C/A | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 113009024 | intron variant | G/A | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 112952224 | intron variant | A/G | snv | 0.57 |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
10 | 113129502 | 5 prime UTR variant | T/A | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 10 | 112971038 | intron variant | A/G | snv | 0.30 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2012 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 113120792 | intron variant | A/T | snv | 0.57 |
|
Mental Disorders | 0.710 | 1.000 | 2 | 2014 | 2016 | |||||||
|
1.000 | 0.040 | 10 | 113089594 | intron variant | C/T | snv | 0.28 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 10 | 113120792 | intron variant | A/T | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.040 | 10 | 113114260 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.040 | 10 | 113114260 | intron variant | C/A;T | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.040 | 10 | 112948751 | upstream gene variant | C/T | snv | 0.23 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.040 | 10 | 112948751 | upstream gene variant | C/T | snv | 0.23 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 10 | 113028677 | intron variant | C/T | snv | 0.15 |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | 10 | 113151854 | synonymous variant | C/T | snv | 1.6E-05 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 |