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 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.710 | 1.000 | 3 | 2007 | 2009 | |||||||
|
1.000 | 0.120 | 9 | 120881577 | intron variant | T/C | snv | 0.44 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2007 | 2009 | |||||||
|
0.925 | 0.160 | 9 | 120890620 | intron variant | T/C | snv | 0.68 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 2 | 2007 | 2009 | |||||||
|
1.000 | 0.120 | 9 | 120900340 | downstream gene variant | T/C | snv | 0.44 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 |
|
Immune System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.120 | 9 | 120878222 | intron variant | T/C | snv | 0.68 |
|
Immune System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.120 | 9 | 120889023 | intron variant | T/C | snv | 0.45 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.160 | 9 | 120890620 | intron variant | T/C | snv | 0.68 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
9 | 120888256 | intron variant | T/A;G | snv |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 9 | 120890102 | intron variant | T/A;C | snv |
|
Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.120 | 9 | 120903623 | 3 prime UTR variant | T/A | snv | 0.44 |
|
Eye Diseases; Immune System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.120 | 9 | 120873843 | intron variant | C/A | snv | 0.47 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 2 | 2014 | 2019 | |||||||
|
9 | 120871670 | intron variant | A/G | snv | 0.65 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
9 | 120868947 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
9 | 120868947 | intron variant | A/C;G | snv |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
9 | 120881148 | intron variant | -/A;AA;AATA;AATTG | ins | 1.8E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |