rs753724, PLCE1

N. diseases: 4
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.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.882 0.080 10 94291660 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.882 0.080 10 94291660 intron variant G/A;C;T snv 0.020 1.000 2 2012 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.080 10 94291660 intron variant G/A;C;T snv 0.020 1.000 2 2012 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.882 0.080 10 94291660 intron variant G/A;C;T snv 0.010 1.000 1 2012 2012