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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 2 | 211424241 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 2 | 211383719 | missense variant | G/A | snv | 4.0E-05 | 7.0E-06 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.120 | 2 | 212529988 | intron variant | C/G | snv | 0.29 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.710 | 1.000 | 2 | 2015 | 2017 | |||||||
|
0.851 | 0.120 | 2 | 212432139 | intron variant | T/C | snv | 0.10 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.710 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.120 | 2 | 212432139 | intron variant | T/C | snv | 0.10 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.710 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 2 | 211668083 | intron variant | A/G | snv | 7.4E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 211676652 | intron variant | C/T | snv | 0.71 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 211521195 | intron variant | A/G | snv | 3.9E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 2 | 211813206 | intron variant | A/G;T | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 211813206 | intron variant | A/G;T | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 212072166 | intron variant | T/C | snv | 0.62 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
2 | 212324070 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1.000 | 0.040 | 2 | 211673690 | intron variant | T/G | snv | 9.6E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 212537150 | intron variant | C/G | snv | 1.7E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 212418466 | intron variant | T/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.851 | 0.080 | 2 | 212050001 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.851 | 0.080 | 2 | 212050001 | intron variant | C/A;T | snv |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 2 | 212050001 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.851 | 0.080 | 2 | 212050001 | intron variant | C/A;T | snv |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
2 | 211440116 | intron variant | A/G | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 2 | 211574587 | intron variant | T/A;C;G | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
2 | 212252904 | intron variant | C/T | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 2 | 211702102 | missense variant | C/T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.120 | 2 | 212527042 | intron variant | G/A;T | snv |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
2 | 212467655 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |