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 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Respiratory Tract Diseases; Cardiovascular Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Respiratory Tract Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
Respiratory Tract Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.120 | 1 | 25808707 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.120 | 1 | 25809731 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 |