rs12498658

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
rs12498658 4:100237821 4q23 G/A 0.1 2.25E-07 1.44 (1.25-1.65) intronic ADH1B Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls