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 | 0.080 | 14 | 68536271 | intron variant | A/G | snv | 0.49 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.882 | 0.080 | 14 | 68536271 | intron variant | A/G | snv | 0.49 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.882 | 0.080 | 14 | 68536271 | intron variant | A/G | snv | 0.49 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.807 | 0.120 | 14 | 68232877 | intron variant | C/T | snv | 0.13 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.830 | 1.000 | 4 | 2012 | 2019 | |||||||
|
1.000 | 0.040 | 14 | 68318360 | intron variant | G/A | snv | 0.54 |
|
Eye Diseases | 0.830 | 1.000 | 4 | 2013 | 2019 | |||||||
|
0.851 | 0.120 | 14 | 68564567 | intron variant | T/A;C | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.030 | 0.667 | 3 | 2010 | 2019 | ||||||||
|
0.851 | 0.120 | 14 | 68564567 | intron variant | T/A;C | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.030 | 0.667 | 3 | 2010 | 2019 | ||||||||
|
0.807 | 0.120 | 14 | 68232877 | intron variant | C/T | snv | 0.13 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.030 | 1.000 | 3 | 2015 | 2019 | |||||||
|
0.925 | 0.160 | 14 | 68293424 | intron variant | C/G;T | snv |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
14 | 68682711 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 2 | 2018 | 2019 | |||||||||||
|
1.000 | 0.080 | 14 | 68276590 | intron variant | A/G;T | snv |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
14 | 68026441 | intron variant | G/A | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 68026441 | intron variant | G/A | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 68439257 | intron variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 68664876 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
14 | 68406810 | intron variant | T/G | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.080 | 14 | 68287978 | intron variant | G/A | snv | 0.57 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 14 | 68287978 | intron variant | G/A | snv | 0.57 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.160 | 14 | 68293424 | intron variant | C/G;T | snv |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.160 | 14 | 68293424 | intron variant | C/G;T | snv |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.807 | 0.160 | 14 | 68193711 | intron variant | T/C | snv | 0.80 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
14 | 67956498 | intron variant | G/A | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 68410812 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.807 | 0.320 | 14 | 68283210 | intron variant | G/A | snv | 0.43 |
|
Endocrine System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
14 | 68455304 | intron variant | T/C | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |