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 | 15 | 39588157 | synonymous variant | C/T | snv | 0.16 | 0.21 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.925 | 0.040 | 15 | 39588157 | synonymous variant | C/T | snv | 0.16 | 0.21 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 15 | 39590289 | intron variant | C/T | snv | 0.12 |
|
Infections; Nervous System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.882 | 0.080 | 15 | 39588621 | missense variant | A/C;G | snv | 4.0E-06; 0.16 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.080 | 15 | 39588621 | missense variant | A/C;G | snv | 4.0E-06; 0.16 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.080 | 15 | 39588621 | missense variant | A/C;G | snv | 4.0E-06; 0.16 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.080 | 15 | 39588621 | missense variant | A/C;G | snv | 4.0E-06; 0.16 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 15 | 39587316 | intron variant | C/A;G;T | snv | 4.2E-06; 0.29 |
|
Infections; Nervous System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.080 | 15 | 39595647 | 3 prime UTR variant | G/A | snv | 0.14 | 0.12 |
|
Infections; Nervous System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.925 | 0.080 | 15 | 39582202 | missense variant | G/C | snv | 6.3E-05 |
|
Immune System Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.925 | 0.080 | 15 | 39582202 | missense variant | G/C | snv | 6.3E-05 |
|
0.010 | 1.000 | 1 | 2003 | 2003 | ||||||||
|
0.882 | 0.120 | 15 | 39580382 | upstream gene variant | T/C | snv | 0.41 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.120 | 15 | 39580382 | upstream gene variant | T/C | snv | 0.41 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.120 | 15 | 39580382 | upstream gene variant | T/C | snv | 0.41 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 15 | 39584048 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.925 | 0.120 | 15 | 39584048 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.925 | 0.120 | 15 | 39584048 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.040 | 0.750 | 4 | 2002 | 2015 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.040 | 0.750 | 4 | 2002 | 2011 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.020 | 0.500 | 2 | 2003 | 2011 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.020 | 0.500 | 2 | 2003 | 2011 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.763 | 0.200 | 15 | 39589977 | missense variant | A/G | snv | 7.9E-02 | 8.0E-02 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 |