Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.820 0.667 1 2013 2016
dbSNP: rs9257809
rs9257809
OR5V1 ; OR12D3
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.820 1.000 1 2012 2017
dbSNP: rs9936833
rs9936833 		0.882 0.160 16 86369512 intergenic variant C/T snv 0.64
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.820 1.000 1 2012 2017
dbSNP: rs10419226
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.800 1.000 1 2013 2013
dbSNP: rs6449586
rs6449586 		1.000 0.080 5 51339044 intergenic variant C/T snv 0.64
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.800 1.000 1 2013 2013