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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.830 | 1.000 | 5 | 2008 | 2013 | |||||||
|
0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 3 | 2008 | 2013 | |||||||
|
0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 |
|
Neoplasms; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 |
|
Male Urogenital Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.851 | 0.160 | 2 | 111098716 | non coding transcript exon variant | A/G | snv | 0.26 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.160 | 2 | 111098716 | non coding transcript exon variant | A/G | snv | 0.26 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.160 | 2 | 111098716 | non coding transcript exon variant | A/G | snv | 0.26 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.160 | 2 | 111098716 | non coding transcript exon variant | A/G | snv | 0.26 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.160 | 2 | 110842129 | intron variant | G/A | snv | 0.44 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.160 | 2 | 110842129 | intron variant | G/A | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.160 | 2 | 110842129 | intron variant | G/A | snv | 0.44 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.120 | 2 | 111074216 | intron variant | T/C | snv | 0.13 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 2 | 2016 | 2017 | |||||||
|
0.925 | 0.120 | 2 | 111074216 | intron variant | T/C | snv | 0.13 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 2 | 2016 | 2017 | |||||||
|
0.925 | 0.120 | 2 | 110858527 | intron variant | G/A | snv | 0.19 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 110858527 | intron variant | G/A | snv | 0.19 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 111114320 | non coding transcript exon variant | G/A | snv | 0.42 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.800 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 2 | 111114320 | non coding transcript exon variant | G/A | snv | 0.42 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 2 | 111061081 | intron variant | A/C | snv | 0.25 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.120 | 2 | 111061081 | intron variant | A/C | snv | 0.25 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.120 | 2 | 110857502 | intron variant | T/G | snv | 0.67 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.120 | 2 | 110850255 | intron variant | A/G | snv | 0.38 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.790 | 0.080 | 2 | 110970905 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.790 | 0.080 | 2 | 110970905 | intron variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.790 | 0.080 | 2 | 110970905 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 |