rs2213042

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
rs2213042 4:100249210 4q23 T/C 0.25 1.66E-06 1.28 (1.16-1.42) intergenic ADH1B(dist=6611), ADH1C(dist=8439) Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls