rs56948765

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
rs56948765 4:100225336 4q23 G/A 0.08 3.38E-06 1.43 (1.23-1.66) intergenic LOC100507053(dist=2823), ADH1B(dist=2208) Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls