rs2178146, None

N. diseases: 8
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.
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.700 1.000 1 2013 2013
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.700 1.000 1 2013 2013
Digestive System Disorders
CUI: C0012242
Disease: Digestive System Disorders
13 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.700 1.000 1 2013 2013
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.700 1.000 1 2013 2013
Intestinal Diseases
CUI: C0021831
Disease: Intestinal Diseases
13 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.700 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.010 1.000 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 0.010 1.000 1 2017 2017