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. 2021 Feb 19;12:1146. doi: 10.1038/s41467-021-21280-7

Table 2.

Genome-wide significant SNPs associated with PUD in the UK Biobank.

Digestion phenotypes SNP* CHR. BP A1/A2 A1 frequency OR P Nearby genes Digestive diseases pleiotropy§ Mental health pleiotropy§
PUD rs681343 19 49206462 C/T 0.49 0.92 1.9E−15 FUT2 Diarrheal disease, Crohn’s disease, IBD, and Gallstone disease
rs2976388 8 143760256 G/A 0.58 1.09 1.8E−14 PSCA Duodenal ulcer, gastric atrophy, and gastric cancer
rs10500661 11 6273744 T/C 0.80 0.90 4.1E−14 CCKBR
rs147048677 1 155161794 C/T 0.94 0.86 9.0E−12 MUC1
rs78459074 11 1029905 A/G 0.89 1.12 2.6E−10 MUC6
rs34074411 17 39867248 C/T 0.56 0.93 2.6E−10 GAST
rs687621 9 136137065 A/G 0.68 1.08 1.3E−09 ABO Duodenal ulcer, Gastric cancer, and pancreatic cancer
rs9581957 13 28557889 C/T 0.68 0.93 3.6E−09 CDX2

*Locus zoom plot for SNPs are in Supplementary Fig. 4.

Odds ratio (OR) is for risk of A1 allele compared to A2 allele.

We note that we do not have direct evidence to support the nearby genes as causal genes, except when linked to gene expression (see Summary data-based Mendelian randomization analysis at the links to gene expression, eQTLs, and mQTLs section).

§We only annotated SNPs if there are SNPs reported associated with either mental health-related traits or digestive diseases from GWAS Catalog in linkage disequilibrium with our UKB digestion SNPs (see “Methods” section and Supplementary Data 1 for detailed description).

IBD inflammatory bowel diseases.