rs10005290

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
rs10005290 4:100229410 4q23 A/C 0.21 1.14E-08 1.35 (1.22-1.5) intronic ADH1B Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls