rs12953717, SMAD7

N. diseases: 18
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 0.724 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
CUI: C0006826
Disease: 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
CUI: C0007102
Disease: 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
CUI: C1306459
Disease: 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
CUI: C1319315
Disease: 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
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.724 0.240 18 48927559 intron variant C/T snv 0.36 0.010 1 2008 2008
Colon Carcinoma
CUI: C0699790
Disease: 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
CUI: C0009375
Disease: 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
CUI: C0009404
Disease: 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
CUI: C0007134
Disease: 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