rs3802842, COLCA2;COLCA1

N. diseases: 25
Source: ALL
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
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.900 1.000 24 2008 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.720 1.000 9 2008 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
Malignant neoplasm of large intestine
375 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 8 2008 2019
Hereditary Nonpolyposis Colorectal Cancer
1331 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.030 1.000 3 2011 2013
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.030 1.000 3 2011 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.020 1.000 2 2008 2013
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.020 1.000 2 2010 2010
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2015 2015
Alcohol or Other Drugs use
CUI: C0237123
Disease: Alcohol or Other Drugs use
21 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2017 2017
Colonic Diseases
CUI: C0009373
Disease: Colonic Diseases
8 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2015 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2015 2015
Malignant neoplasm of colon and/or rectum
502 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2015 2015
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.700 1.000 1 2010 2010
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2017 2017
Rectal Diseases
CUI: C0034882
Disease: Rectal Diseases
3 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012
Rectal Neoplasms
CUI: C0034885
Disease: Rectal Neoplasms
21 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012