rs2066701

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
rs2066701 4:100238413 4q23 G/A 0.21 7.14E-09 1.36 (1.22-1.51) intronic ADH1B Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls