rs3762896

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
rs3762896 4:100268131 4q23 C/T 0.24 2.32E-06 1.28 (1.15-1.41) intronic ADH1C Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls