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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.040 | 7 | 40426601 | intron variant | C/T | snv | 0.12 |
|
Nervous System Diseases | 0.830 | 1.000 | 4 | 2013 | 2019 | |||||||
|
1.000 | 0.080 | 7 | 40459197 | missense variant | C/T | snv | 4.6E-03 | 4.8E-03 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 2 | 2008 | 2014 | ||||||
|
0.925 | 0.040 | 7 | 40426601 | intron variant | C/T | snv | 0.12 |
|
Nervous System Diseases | 0.720 | 1.000 | 3 | 2013 | 2019 | |||||||
|
1.000 | 0.120 | 7 | 40827064 | intron variant | C/A | snv | 0.20 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.700 | 1.000 | 2 | 2015 | 2018 | |||||||
|
7 | 40304762 | intron variant | C/A;G | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
7 | 40822846 | intron variant | A/G | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.080 | 7 | 40133169 | missense variant | T/C | snv | 2.8E-05 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||||
|
1.000 | 7 | 40294343 | intron variant | T/G | snv | 8.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 7 | 40294343 | intron variant | T/G | snv | 8.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 7 | 40294343 | intron variant | T/G | snv | 8.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 7 | 40294343 | intron variant | T/G | snv | 8.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 7 | 40294343 | intron variant | T/G | snv | 8.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
7 | 40376718 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 7 | 40835593 | intron variant | A/C | snv | 0.21 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
7 | 40367277 | intron variant | A/C;G;T | snv |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
7 | 40776866 | intron variant | C/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 40322235 | intron variant | G/C | snv | 0.68 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
7 | 40322235 | intron variant | G/C | snv | 0.68 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
7 | 40378133 | intron variant | G/- | del | 0.81 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
7 | 40408372 | intron variant | G/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 7 | 40834777 | intron variant | G/T | snv | 0.24 |
|
Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 7 | 40134228 | splice donor variant | C/A;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 7 | 40237664 | stop gained | C/A;T | snv | 1.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 7 | 40133169 | missense variant | T/C | snv | 2.8E-05 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||
|
1.000 | 0.080 | 7 | 40134482 | missense variant | C/T | snv | 4.5E-05 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 0 |