rs4925386, LAMA5

N. diseases: 14
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 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.830 1.000 3 2010 2018
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.010 1 2013 2013
Colonic Diseases
CUI: C0009373
Disease: Colonic Diseases
8 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.010 1.000 1 2012 2012
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016