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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
Digestive System Diseases; Neoplasms | 0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
Digestive System Diseases; Neoplasms | 0.010 | < 0.001 | 1 | 2014 | 2014 | |||||||
|
0.790 | 0.080 | 17 | 78855710 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2014 | 2014 | ||||||||
|
17 | 78856015 | 3 prime UTR variant | G/A | snv | 0.71 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
0.010 | < 0.001 | 1 | 2017 | 2017 | ||||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.010 | < 0.001 | 1 | 2012 | 2012 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.752 | 0.280 | 17 | 78925807 | upstream gene variant | C/G | snv | 1.6E-02 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.200 | 17 | 78925567 | upstream gene variant | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.200 | 17 | 78925567 | upstream gene variant | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.200 | 17 | 78925567 | upstream gene variant | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.200 | 17 | 78925567 | upstream gene variant | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 |