rs2866149

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
rs2866149 4:100190732 4q23 C/G 0.11 3.74E-06 1.37 (1.2-1.57) ncRNA_intronic LOC100507053 Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls