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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.080 | 10 | 112962862 | intron variant | G/A;C | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.160 | 10 | 112976855 | intron variant | T/C | snv | 0.20 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 10 | 113022528 | intron variant | T/G | snv | 6.1E-02 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
10 | 113153211 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.160 | 10 | 113029056 | intron variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.160 | 10 | 113029056 | intron variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.040 | 10 | 113120792 | intron variant | A/T | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
10 | 113144442 | intron variant | T/G | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.160 | 10 | 112992744 | intron variant | T/C | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.160 | 10 | 112992744 | intron variant | T/C | snv | 0.17 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.160 | 10 | 112992744 | intron variant | T/C | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
10 | 112955839 | intron variant | G/A | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
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 | ||||||||
|
0.827 | 0.200 | 10 | 113164066 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 10 | 112994312 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
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 | ||||||||||
|
1.000 | 0.080 | 10 | 112988102 | intron variant | GT/-;GTGT;GTGTGT | delins |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 10 | 113008012 | intron variant | G/A | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
10 | 113035497 | intron variant | G/C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 |