Disease | N. SNPs d | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AFEXOME | AFGENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Aplastic Anemia
|
16 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
Arthritis, Psoriatic
|
50 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
Behcet Syndrome
|
202 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
Colon Carcinoma
|
275 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
Gastritis
|
18 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
Graves Disease
|
252 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
Laryngeal Squamous Cell Carcinoma
|
24 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
Malignant Neoplasms
|
1441 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
Malignant tumor of colon
|
289 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
Non-Small Cell Lung Carcinoma
|
601 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
Pituitary Adenoma
|
8 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
Primary malignant neoplasm
|
1374 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
Stomatitis
|
22 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
Multiple Sclerosis
|
448 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.820 | 1.000 | 2 | 2010 | 2012 | |||||
Hashimoto Disease
|
115 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.020 | 1.000 | 2 | 2014 | 2015 | |||||
Malignant neoplasm of stomach
|
603 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.020 | 1.000 | 2 | 2014 | 2015 | |||||
Neoplasms
|
1571 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.020 | 1.000 | 2 | 2014 | 2016 | |||||
Stomach Carcinoma
|
616 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.020 | 1.000 | 2 | 2014 | 2015 | |||||
Ulcerative Colitis
|
392 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.030 | 1.000 | 3 | 2012 | 2014 | |||||
Crohn Disease
|
456 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 0.870 | 1.000 | 7 | 2008 | 2016 |