rs2032348

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
rs2032348 4:100064247 4q23 G/T 0.31 1.81E-11 1.39 (1.26-1.53) ncRNA_intronic LOC100507053 Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls