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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 3 | 8745701 | missense variant | T/G | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.820 | 1.000 | 4 | 2006 | 2018 | ||||||||
|
0.882 | 0.200 | 3 | 8733956 | missense variant | G/A;C | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.800 | 1.000 | 14 | 2000 | 2011 | ||||||||
|
0.827 | 0.160 | 3 | 8745725 | missense variant | C/T | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.800 | 1.000 | 12 | 1998 | 2006 | ||||||||
|
1.000 | 0.120 | 3 | 8745834 | missense variant | C/G | snv | 8.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2006 | 2007 | |||||||
|
1.000 | 0.120 | 3 | 8745664 | missense variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2006 | 2007 | ||||||||
|
0.925 | 0.120 | 3 | 8745647 | missense variant | T/G | snv | 1.4E-05 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2006 | 2007 | |||||||
|
0.925 | 0.080 | 3 | 8745548 | missense variant | C/A;T | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.800 | 0 | |||||||||||
|
0.882 | 0.200 | 3 | 8733956 | missense variant | G/A;C | snv |
|
0.800 | 0 | ||||||||||||
|
0.925 | 0.080 | 3 | 8733960 | missense variant | C/A | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.800 | 0 | |||||||||||
|
3 | 8733962 | missense variant | C/A;T | snv |
|
0.800 | 0 | ||||||||||||||
|
0.925 | 0.080 | 3 | 8745547 | missense variant | G/A;T | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.800 | 0 | |||||||||||
|
0.807 | 0.200 | 3 | 8745644 | missense variant | C/A;T | snv | 4.0E-06; 2.6E-03 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.800 | 0 | ||||||||||
|
0.882 | 0.200 | 3 | 8733956 | missense variant | G/A;C | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 14 | 2000 | 2011 | ||||||||
|
0.925 | 0.120 | 3 | 8745601 | missense variant | A/C | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 1.000 | 12 | 1998 | 2006 | ||||||||
|
1.000 | 0.080 | 3 | 8745602 | missense variant | C/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 6 | 2004 | 2017 | ||||||||
|
1.000 | 0.120 | 3 | 8745580 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 3 | 2004 | 2017 | ||||||
|
0.851 | 0.200 | 3 | 8745688 | missense variant | G/A;T | snv | 1.6E-04; 2.0E-05 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 1.000 | 3 | 2003 | 2010 | |||||||
|
0.851 | 0.200 | 3 | 8745688 | missense variant | G/A;T | snv | 1.6E-04; 2.0E-05 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 2 | 2003 | 2005 | |||||||
|
0.925 | 0.120 | 3 | 8733916 | missense variant | G/A;C | snv | 4.3E-04 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.925 | 0.120 | 3 | 8745647 | missense variant | T/G | snv | 1.4E-05 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.080 | 3 | 8733976 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.882 | 0.120 | 3 | 8733975 | missense variant | C/A;G;T | snv | 0.29 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 3 | 8733975 | missense variant | C/A;G;T | snv | 0.29 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.120 | 3 | 8733882 | frameshift variant | GG/- | del | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.200 | 3 | 8733956 | missense variant | G/A;C | snv |
|
0.700 | 0 |