rs3784262, ALDH1A2

N. diseases: 6
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.
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.882 0.160 15 57960908 intron variant T/A;C snv 0.820 0.667 3 2013 2016
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.882 0.160 15 57960908 intron variant T/A;C snv 0.710 1.000 2 2013 2015
Digestive System Disorders
CUI: C0012242
Disease: Digestive System Disorders
13 0.882 0.160 15 57960908 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.882 0.160 15 57960908 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Intestinal Diseases
CUI: C0021831
Disease: Intestinal Diseases
13 0.882 0.160 15 57960908 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.882 0.160 15 57960908 intron variant T/A;C snv 0.010 1 2016 2016