rs10031168

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
rs10031168 4:100281893 4q23 T/C 0.24 1.93E-06 1.28 (1.16-1.41) intergenic ADH1C(dist=7691), ADH7(dist=51525) Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls