rs17028609

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
rs17028609 4:100070885 4q23 G/A 0.3 1.06E-12 1.42 (1.29-1.56) ncRNA_intronic LOC100507053 Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls