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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.080 | 13 | 28301652 | 3 prime UTR variant | A/C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 13 | 28301652 | 3 prime UTR variant | A/C | snv |
|
Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 13 | 28301652 | 3 prime UTR variant | A/C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 13 | 28301652 | 3 prime UTR variant | A/C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 13 | 28302077 | 3 prime UTR variant | T/C | snv | 0.21 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28302077 | 3 prime UTR variant | T/C | snv | 0.21 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28302077 | 3 prime UTR variant | T/C | snv | 0.21 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28302077 | 3 prime UTR variant | T/C | snv | 0.21 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28305702 | intron variant | G/A | snv | 0.54 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.851 | 0.080 | 13 | 28305702 | intron variant | G/A | snv | 0.54 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28305702 | intron variant | G/A | snv | 0.54 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.851 | 0.080 | 13 | 28305702 | intron variant | G/A | snv | 0.54 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.120 | 13 | 28308924 | synonymous variant | G/A | snv | 0.80 | 0.67 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.925 | 0.120 | 13 | 28308924 | synonymous variant | G/A | snv | 0.80 | 0.67 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.030 | 1.000 | 3 | 2014 | 2017 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
0.030 | 1.000 | 3 | 2014 | 2017 | ||||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.280 | 13 | 28311271 | intron variant | C/A | snv | 0.59 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.882 | 0.160 | 13 | 28312790 | intron variant | A/C;G | snv |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.030 | 1.000 | 3 | 2014 | 2017 | ||||||||
|
0.882 | 0.160 | 13 | 28312790 | intron variant | A/C;G | snv |
|
0.030 | 1.000 | 3 | 2014 | 2017 | |||||||||
|
0.882 | 0.160 | 13 | 28312790 | intron variant | A/C;G | snv |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 |