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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.160 | 11 | 111908841 | stop gained | G/A;C | snv |
|
Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 11 | 111908822 | missense variant | C/T | snv | 7.2E-05 | 4.9E-05 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.160 | 11 | 111908827 | frameshift variant | AG/- | del |
|
Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 11 | 111908842 | frameshift variant | T/- | delins |
|
0.700 | 0 | |||||||||||||
|
11 | 111908969 | splice acceptor variant | T/C | snv | 3.6E-05 | 2.1E-05 |
|
Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 11 | 111911665 | frameshift variant | G/- | delins |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 11 | 111911665 | frameshift variant | G/- | delins |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 11 | 111908949 | frameshift variant | A/- | del | 4.0E-06 | 1.4E-05 |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||
|
1.000 | 11 | 111908874 | missense variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 11 | 111911667 | missense variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
0.827 | 0.200 | 11 | 111911559 | missense variant | G/A;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.280 | 11 | 111908967 | missense variant | C/A;G | snv |
|
Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
11 | 111911722 | start lost | C/T | snv | 6.7E-05 | 2.8E-05 |
|
Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Cardiovascular Diseases | 0.060 | 1.000 | 6 | 2005 | 2019 | ||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Eye Diseases | 0.040 | 1.000 | 4 | 2011 | 2019 | ||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.800 | 1.000 | 4 | 1998 | 2012 | ||||||||
|
0.882 | 0.040 | 11 | 111908966 | missense variant | T/C | snv |
|
0.700 | 1.000 | 4 | 2012 | 2017 | |||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.030 | 1.000 | 3 | 2002 | 2011 | ||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Musculoskeletal Diseases; Nervous System Diseases | 0.030 | 1.000 | 3 | 2005 | 2014 | ||||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Eye Diseases | 0.020 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
0.807 | 0.240 | 11 | 111908832 | missense variant | C/T | snv | 9.1E-04 | 8.7E-04 |
|
0.800 | 1.000 | 2 | 2006 | 2006 | |||||||
|
0.807 | 0.240 | 11 | 111908832 | missense variant | C/T | snv | 9.1E-04 | 8.7E-04 |
|
Eye Diseases | 0.020 | 1.000 | 2 | 2010 | 2017 | ||||||
|
0.925 | 0.080 | 11 | 111908949 | frameshift variant | A/- | del | 4.0E-06 | 1.4E-05 |
|
0.700 | 1.000 | 2 | 2011 | 2016 | |||||||
|
0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 |