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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Liver carcinoma
|
942 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
Malignant Neoplasms
|
1641 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.030 | 1.000 | 3 | 2011 | 2015 | ||||
Primary malignant neoplasm
|
1374 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.030 | 1.000 | 3 | 2011 | 2015 | ||||
Colorectal Carcinoma
|
1962 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
Malignant neoplasm of stomach
|
615 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
Stomach Carcinoma
|
652 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
Carcinoma, Ovarian Epithelial
|
327 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
Malignant neoplasm of ovary
|
315 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
ovarian neoplasm
|
757 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
Head and Neck Carcinoma
|
118 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
Malignant Head and Neck Neoplasm
|
118 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
Complete Trisomy 21 Syndrome
|
77 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.020 | 1.000 | 2 | 2015 | 2018 | ||||
Down Syndrome
|
80 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.020 | 1.000 | 2 | 2015 | 2018 | ||||
Graves Disease
|
352 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
Immune thrombocytopenic purpura
|
35 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
Parkinson Disease
|
990 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.020 | 1.000 | 2 | 2017 | 2017 | ||||
Nonorganic psychosis
|
98 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
Psychotic Disorders
|
179 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 0.010 | 1.000 | 1 | 2017 | 2017 |