rs4939827, SMAD7

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 0.708 0.160 18 48927093 intron variant T/A;C snv 0.900 0.964 28 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.708 0.160 18 48927093 intron variant T/A;C snv 0.800 1.000 8 2007 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.708 0.160 18 48927093 intron variant T/A;C snv 0.750 1.000 12 2007 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 1 2010 2010
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.708 0.160 18 48927093 intron variant T/A;C snv 0.070 1.000 7 2009 2017
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.708 0.160 18 48927093 intron variant T/A;C snv 0.050 1.000 5 2008 2016
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.708 0.160 18 48927093 intron variant T/A;C snv 0.020 1.000 2 2012 2016
Alcohol or Other Drugs use
CUI: C0237123
Disease: Alcohol or Other Drugs use
21 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2012 2012
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2009 2009
Drug usage
CUI: C0242510
Disease: Drug usage
21 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2010 2010
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1 2011 2011
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1 2011 2011
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2016 2016