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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 1 | 155904472 | missense variant | T/C | snv |
|
0.700 | 0 | |||||||||||||
|
0.882 | 0.160 | 1 | 155910693 | missense variant | T/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 1 | 155910693 | missense variant | T/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 1 | 155910693 | missense variant | T/G | snv |
|
Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Respiratory Tract Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Female Urogenital Diseases and Pregnancy Complications | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Female Urogenital Diseases and Pregnancy Complications | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Respiratory Tract Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
Respiratory Tract Diseases | 0.700 | 0 | |||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
Mental Disorders | 0.700 | 0 | |||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
Respiratory Tract Diseases | 0.700 | 0 | |||||||||||
|
0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv |
|
Cardiovascular Diseases | 0.700 | 0 |