rs58223772

Genome Assembly: GRCh37.p13/hg19

External References:


Association with risk of ESCC

in 2,022 ESCC cases and 2,039 controls

SNPLocationRegionAlleleMAFP-valueOR(95% CI)Functional
class
Mapped
gene(s)
Study
rs58223772 4:100256165 4q23 TC/T 0.25 1.87E-06 1.28 (1.16-1.41) intergenic ADH1B(dist=13565), ADH1C(dist=1484) Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls