Trait
SNPs associated with Esophageal Disease
13 genetic variants across 6 genes have been associated with Esophageal Disease in published research. Key genes include APOE, ATXN2, CRTC1.
Associated variants13 total
| rsid | Gene | Effect | Evidence |
|---|---|---|---|
| rs4766578 | ATXN2 | GWAS association (p=4.0e-16) | Major Consortium Study |
| rs10987077 | — | GWAS association (p=3.0e-13) | Major Consortium Study |
| rs11863156 | — | GWAS association (p=4.0e-13) | Major Consortium Study |
| rs6499626 | — | GWAS association (p=7.0e-13) | Major Consortium Study |
| rs429358 | APOE | GWAS association (p=4.0e-12) | Major Consortium Study |
| rs566890996 | FYB2 | GWAS association (p=8.0e-12) | Major Consortium Study |
| rs13107325 | SLC39A8 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs10404696 | CRTC1 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs2891698 | — | GWAS association (p=3.0e-16) | Major Consortium Study |
| rs9673356 | — | GWAS association (p=7.0e-21) | Major Consortium Study |
| rs3094503 | — | GWAS association (p=3.0e-16) | Large GWAS |
| rs8046904 | — | GWAS association (p=2.0e-10) | Large GWAS |
| rs187017665 | CTNNA3 | GWAS association (p=2.0e-08) | Large GWAS |
Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.