rs7229639, SMAD7

N. diseases: 13
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 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.820 1.000 6 2014 2019
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
Malignant neoplasm of large intestine
375 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.700 1.000 5 2014 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.010 1.000 1 2016 2016
Digestive System Disorders
CUI: C0012242
Disease: Digestive System Disorders
13 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.010 1.000 1 2016 2016
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.010 1.000 1 2014 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.010 1.000 1 2017 2017