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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 0.667 | 3 | 2005 | 2010 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 0.667 | 3 | 2005 | 2010 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 0.667 | 3 | 2005 | 2010 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2004 | 2014 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms | 0.020 | 1.000 | 2 | 2005 | 2015 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2005 | 2016 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.020 | 0.500 | 2 | 1997 | 2018 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2015 | 2017 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2011 | 2014 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.020 | 0.500 | 2 | 2009 | 2015 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.020 | 0.500 | 2 | 2005 | 2006 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms | 0.020 | 1.000 | 2 | 2005 | 2015 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.020 | 0.500 | 2 | 2005 | 2006 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
0.010 | < 0.001 | 1 | 2009 | 2009 | |||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |