DRG1, developmentally regulated GTP binding protein 1, 4733
N. diseases: 43; N. variants: 6
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
22 | 31417072 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
22 | 31417072 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
1.000 | 0.120 | 22 | 31504373 | intron variant | C/A;T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
22 | 31463873 | synonymous variant | A/G | snv | 0.10 | 6.8E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
22 | 31425733 | intron variant | G/A | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 22 | 31488419 | intron variant | T/A;C | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2012 | 2012 |