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 | 0.160 | 7 | 73708593 | synonymous variant | A/G | snv | 0.51 | 0.53 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2017 | 2018 | ||||||
|
0.925 | 0.160 | 7 | 73703866 | 3 prime UTR variant | T/C | snv | 0.42 | 0.32 |
|
Nervous System Diseases | 0.020 | 1.000 | 2 | 2009 | 2012 | ||||||
|
1.000 | 0.040 | 7 | 73712768 | intron variant | G/A | snv | 2.1E-02 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2015 | 2019 | |||||||
|
1.000 | 0.040 | 7 | 73710933 | intron variant | G/A | snv | 0.28 |
|
Nervous System Diseases | 0.020 | 1.000 | 2 | 2009 | 2010 | |||||||
|
1.000 | 0.040 | 7 | 73710933 | intron variant | G/A | snv | 0.28 |
|
Nervous System Diseases | 0.020 | 1.000 | 2 | 2010 | 2012 | |||||||
|
1.000 | 0.080 | 7 | 73700151 | 3 prime UTR variant | C/T | snv | 0.10 |
|
Immune System Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.160 | 7 | 73708593 | synonymous variant | A/G | snv | 0.51 | 0.53 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1.000 | 0.080 | 7 | 73708593 | synonymous variant | A/G | snv |
|
Nervous System Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.925 | 0.080 | 7 | 73707017 | intron variant | A/G | snv | 0.55 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.925 | 0.080 | 7 | 73707017 | intron variant | A/G | snv | 0.55 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.160 | 7 | 73703866 | 3 prime UTR variant | T/C | snv | 0.42 | 0.32 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.925 | 0.160 | 7 | 73703866 | 3 prime UTR variant | T/C | snv | 0.42 | 0.32 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Nervous System Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 7 | 73718911 | intron variant | T/G | snv | 0.21 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.040 | 7 | 73718911 | intron variant | T/G | snv | 0.21 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 |