rs1800469, B9D2;TGFB1

N. diseases: 78
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 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.810 1.000 4 2014 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.710 1.000 4 2011 2016
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 3 2014 2016
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.700 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.040 0.750 4 2012 2019
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.040 1.000 4 2004 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.040 0.750 4 2012 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 0.500 2 2013 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2012 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2012 2012
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2017 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2012 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2006 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2015 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.020 1.000 2 2012 2019
Acquired aplastic anemia
CUI: C0271907
Disease: Acquired aplastic anemia
12 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2017 2017
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2015 2015
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2013 2013
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2015 2015