443 positions on this site are linked to Glaucoma, out of 103,694 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
FNDC3B · rs16845236
See detailed info → Standardnear EYA1 · rs10504513
See detailed info → StandardCADM2 · rs9819278
See detailed info → StandardGSX2 · rs4864858
See detailed info → StandardLYPLAL1-DT · rs6697647
See detailed info → StandardRIC8B · rs66716938
See detailed info → StandardGAS7 · rs12602519
See detailed info → StandardRUNX1 · rs10483029
See detailed info → StandardTXNRD2 · rs1044732
See detailed info → Standardnear SRSF3 · rs10947614
See detailed info → StandardRALGPS1 · rs955934
See detailed info → StandardPXDNL · rs11984688
See detailed info → StandardEGLN3 · rs10139172
See detailed info → StandardLMO7 · rs9544026
See detailed info → StandardRFX4 · rs7954897
See detailed info → Standardnear MYO16 · rs7338021
See detailed info → StandardLINC01349 · rs34202160
See detailed info → StandardPRSS23 · rs2105587
See detailed info → StandardCADM2 · rs13064817
See detailed info → StandardCAV2 · rs12540035
See detailed info →Showing 20 of 443 · page 6 of 23
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.