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 | 1 | 10258602 | missense variant | A/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1 | 10297206 | missense variant | A/T | snv |
|
0.700 | 0 | ||||||||||||||
|
1.000 | 0.040 | 1 | 10365476 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
Neoplasms | 0.700 | 0 | |||||||||
|
1.000 | 0.040 | 1 | 10365476 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.120 | 1 | 10378834 | 3 prime UTR variant | G/A | snv | 0.33 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.120 | 1 | 10378834 | 3 prime UTR variant | G/A | snv | 0.33 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
Digestive System Diseases; Infections | 0.730 | 0.750 | 4 | 2011 | 2019 | |||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.900 | 0.833 | 12 | 2010 | 2019 | |||||||
|
1.000 | 0.080 | 1 | 10293054 | intron variant | T/C | snv | 0.32 |
|
Immune System Diseases; Nervous System Diseases | 0.830 | 1.000 | 4 | 2008 | 2011 | |||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
0.020 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
1 | 10211630 | 5 prime UTR variant | C/G | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 10297748 | intron variant | G/C | snv | 5.8E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 10297748 | intron variant | G/C | snv | 5.8E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.882 | 0.080 | 1 | 10258602 | missense variant | A/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.800 | 1.000 | 1 | 2001 | 2001 | ||||||||
|
0.882 | 0.080 | 1 | 10258602 | missense variant | A/T | snv |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.882 | 0.080 | 1 | 10258602 | missense variant | A/T | snv |
|
0.010 | 1.000 | 1 | 2004 | 2004 | |||||||||
|
1 | 10345943 | missense variant | C/T | snv | 2.0E-04 | 5.6E-05 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
1.000 | 0.080 | 1 | 10295763 | missense variant | G/A | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||||
|
1 | 10297069 | missense variant | G/A | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1 | 10226118 | intron variant | G/A;C | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1 | 10226118 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
1 | 10226118 | intron variant | G/A;C | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 |