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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Colorectal Carcinoma
|
1962 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.900 | 1.000 | 14 | 2007 | 2018 | |||||
Malignant neoplasm of colon and/or rectum
|
502 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.060 | 1.000 | 6 | 2008 | 2014 | |||||
Malignant Neoplasms
|
1641 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.020 | 1.000 | 2 | 2011 | 2013 | |||||
Malignant tumor of colon
|
688 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.710 | 1.000 | 2 | 2010 | 2017 | |||||
Primary malignant neoplasm
|
1374 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.020 | 1.000 | 2 | 2011 | 2013 | |||||
Adenocarcinoma of large intestine
|
432 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
Chronic Lymphocytic Leukemia
|
291 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1 | 2008 | 2008 | ||||||
Colon Carcinoma
|
275 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
Colonic Neoplasms
|
45 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
|
374 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
|
370 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
|
373 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
|
368 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
Colorectal Neoplasms
|
609 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
Conventional (Clear Cell) Renal Cell Carcinoma
|
222 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
Malignant neoplasm of large intestine
|
375 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
Renal Cell Carcinoma
|
288 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
Squamous cell carcinoma of esophagus
|
329 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.010 | 1 | 2017 | 2017 |