rs717746, CDX1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
0.010 GeneticVariation BEFREE Five variants of Cdx1 SNPs (rs3776082, rs717746 and rs3776083), one Cdx1 haplotype, and three variants of Cdx2 SNPs (rs4769585 and rs3812863) were associated with BE (P < 0.05). 23918153 2014