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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.742 | 0.280 | 16 | 1079872 | missense variant | C/T | snv | 0.54 | 0.50 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.925 | 0.080 | 16 | 1081695 | upstream gene variant | A/C;G | snv |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.080 | 16 | 1081695 | upstream gene variant | A/C;G | snv |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.120 | 16 | 1079501 | synonymous variant | C/T | snv | 5.9E-02 | 4.8E-02 |
|
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.827 | 0.080 | 16 | 1079441 | synonymous variant | G/A | snv | 1.7E-02 | 1.5E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||
|
0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | < 0.001 | 1 | 2009 | 2009 |