rs5277, PACERR;PTGS2

N. diseases: 9
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.030 0.667 3 2010 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.030 0.667 3 2010 2015
Pain
CUI: C0030193
Disease: Pain
196 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.020 1.000 2 2012 2015
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2009 2009
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2014 2014
Left main coronary artery disease
CUI: C1299433
Disease: Left main coronary artery disease
4 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2017 2017
Malignant neoplasm of colon and/or rectum
502 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2009 2009
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 0.010 1.000 1 2009 2009