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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.160 | 6 | 31962685 | intron variant | G/A | snv | 0.14 | 0.16 |
|
Eye Diseases | 0.870 | 1.000 | 12 | 2010 | 2019 | ||||||
|
1.000 | 6 | 31962012 | missense variant | T/G | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.882 | 0.240 | 6 | 31965384 | intron variant | G/A | snv | 0.19 |
|
Eye Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.882 | 0.240 | 6 | 31965384 | intron variant | G/A | snv | 0.19 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 3 | 2007 | 2011 | |||||||
|
0.925 | 0.160 | 6 | 31960529 | missense variant | A/G | snv | 9.7E-02 | 0.12 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 3 | 2007 | 2011 | ||||||
|
0.925 | 0.200 | 6 | 31966595 | intron variant | C/T | snv | 0.19 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 3 | 2007 | 2011 | |||||||
|
0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv |
|
Eye Diseases | 0.700 | 1.000 | 2 | 2016 | 2018 | ||||||||
|
0.882 | 0.160 | 6 | 31961237 | missense variant | A/C | snv | 0.76 | 0.78 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2007 | 2009 | ||||||
|
1.000 | 0.080 | 6 | 31968280 | non coding transcript exon variant | G/T | snv |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
6 | 31964400 | intron variant | C/T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 6 | 31968280 | non coding transcript exon variant | G/T | snv | 7.2E-02 | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 6 | 31968280 | non coding transcript exon variant | G/T | snv | 7.2E-02 | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 6 | 31968280 | non coding transcript exon variant | G/T | snv | 7.2E-02 | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 6 | 31968280 | non coding transcript exon variant | G/T | snv | 7.2E-02 | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 6 | 31963360 | intron variant | T/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1.000 | 6 | 31963360 | intron variant | T/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1.000 | 6 | 31963360 | intron variant | T/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1.000 | 6 | 31963360 | intron variant | T/C | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.882 | 0.240 | 6 | 31965384 | intron variant | G/A | snv | 0.19 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.120 | 6 | 31961022 | intron variant | T/A;C | snv | 0.76 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.882 | 0.160 | 6 | 31961237 | missense variant | A/C | snv | 0.76 | 0.78 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.160 | 6 | 31961237 | missense variant | A/C | snv | 0.76 | 0.78 |
|
Immune System Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 |