rs1800761

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
rs1800761 4:100065593 4q23 T/A,C 0.3 1.26E-11 1.4 (1.27-1.54) ncRNA_intronic LOC100507053 Wu C, et al. (PMID: 21642993), 2011

MAF: minor allele frequency in controls