rs4939827, SMAD7

N. diseases: 10
Source: GWASCAT ×
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
368 0.708 0.160 18 48927093 intron variant T/A;C snv 0.900 0.964 8 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
368 0.708 0.160 18 48927093 intron variant T/A;C snv 0.750 1.000 8 2007 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
368 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
368 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
368 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
368 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
368 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
368 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
1159 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 1 2019 2019