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 | 15 | 32733778 | 3 prime UTR variant | C/T | snv | 0.16 |
|
Digestive System Diseases; Neoplasms | 0.730 | 1.000 | 4 | 2008 | 2015 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.800 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 3 | 2014 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.882 | 0.080 | 15 | 32733778 | 3 prime UTR variant | C/T | snv | 0.16 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.882 | 0.080 | 15 | 32733778 | 3 prime UTR variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.120 | 15 | 32734466 | 3 prime UTR variant | A/T | snv | 0.19 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.120 | 15 | 32731784 | 3 prime UTR variant | A/G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.120 | 15 | 32731180 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.120 | 15 | 32731180 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.790 | 0.080 | 15 | 32718211 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2015 | 2015 |