rs12190287, TCF21

N. diseases: 19
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.820 1.000 4 2011 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.720 1.000 4 2013 2017
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.700 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.700 1.000 1 2013 2013
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2016 2016
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Ductal Breast Carcinoma
CUI: C1527349
Disease: Ductal Breast Carcinoma
10 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2016 2016
Ductal Carcinoma
CUI: C1176475
Disease: Ductal Carcinoma
11 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2016 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017