rs9929218, CDH1

N. diseases: 16
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 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.850 1.000 6 2008 2016
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.710 1.000 2 2008 2013
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
Malignant neoplasm of large intestine
375 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2010 2010
Malignant neoplasm of colon and/or rectum
502 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.020 1.000 2 2015 2016
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2010 2010
Alcohol or Other Drugs use
CUI: C0237123
Disease: Alcohol or Other Drugs use
21 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2012 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2015 2015