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 | 0.040 | 1 | 8699495 | intron variant | T/C | snv | 0.26 |
|
Eye Diseases | 0.010 | < 0.001 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.040 | 1 | 8699495 | intron variant | T/C | snv | 0.26 |
|
Eye Diseases | 0.010 | < 0.001 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.120 | 1 | 8422018 | intron variant | C/T | snv | 0.62 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.851 | 0.120 | 1 | 8422018 | intron variant | C/T | snv | 0.62 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.200 | 1 | 8360264 | synonymous variant | C/A;G;T | snv | 2.3E-05; 5.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||||
|
1.000 | 0.080 | 1 | 8362754 | missense variant | G/A;C | snv | 1.6E-05; 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.120 | 1 | 8358814 | missense variant | C/T | snv | 4.0E-06 |
|
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 1 | 8362757 | missense variant | C/A;T | snv | 3.6E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 1 | 8444361 | intron variant | C/A | snv | 0.52 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||
|
1.000 | 0.040 | 1 | 8435530 | intron variant | A/G | snv | 0.31 |
|
Mental Disorders | 0.700 | 1.000 | 2 | 2017 | 2019 | |||||||
|
1.000 | 0.040 | 1 | 8427263 | intron variant | C/A | snv | 0.30 |
|
Mental Disorders | 0.700 | 1.000 | 2 | 2015 | 2019 | |||||||
|
0.882 | 0.120 | 1 | 8441726 | intron variant | A/G;T | snv |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||
|
1 | 8648470 | intron variant | T/C | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 1 | 8834298 | intron variant | A/T | snv | 0.51 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 8447713 | intron variant | G/A | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.120 | 1 | 8400188 | intron variant | CA/- | del | 0.22 |
|
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 8460428 | intron variant | AAG/- | delins | 0.16 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 8416368 | intron variant | A/G | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 8430923 | intron variant | C/T | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 1 | 8444361 | intron variant | C/A | snv | 0.52 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 1 | 8444361 | intron variant | C/A | snv | 0.52 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 |