rs3781264, PLCE1

N. diseases: 5
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 0.851 0.120 10 94310618 intron variant A/G snv 0.25 0.700 1.000 2 2010 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.851 0.120 10 94310618 intron variant A/G snv 0.25 0.710 1.000 2 2010 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.851 0.120 10 94310618 intron variant A/G snv 0.25 0.010 1.000 1 2012 2012
Dengue Shock Syndrome
CUI: C0376300
Disease: Dengue Shock Syndrome
9 0.851 0.120 10 94310618 intron variant A/G snv 0.25 0.700 1.000 1 2011 2011
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.851 0.120 10 94310618 intron variant A/G snv 0.25 0.010 1.000 1 2012 2012