rs17028765

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
rs17028765 4:100188396 4q23 T/C 0.08 1.33E-06 1.46 (1.25-1.7) ncRNA_intronic LOC100507053 Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls