rs12644388

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
rs12644388 4:100290340 4q23 A/T 0.26 8.90E-06 1.25 (1.13-1.38) intergenic ADH1C(dist=16138), ADH7(dist=43078) Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls