444 positions on this site are linked to Glaucoma, out of 104,072 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CDKN2B-AS1 · rs1412829
See detailed info → StandardBICC1 · rs1658436
See detailed info → Standardnear PFN1P1 · rs144408824
See detailed info → StandardAFAP1 · rs28464089
See detailed info → Standardnear CAV1 · rs10257125
See detailed info → Standardnear PTHLH · rs7972874
See detailed info → StandardLINC01214 · rs11710845
See detailed info → Standardnear PSMC1P4 · rs158638
See detailed info → StandardVAV2 · rs10993828
See detailed info → StandardARHGEF3 · rs9311623
See detailed info → StandardLMX1B-DT · rs6478746
See detailed info → StandardVPS13D · rs6690264
See detailed info → Standardnear LYPLA1P2 · rs17527016
See detailed info → StandardPDE7B · rs9389370
See detailed info → StandardLINC01376 · rs72778322
See detailed info → StandardLINC00540 · rs4769194
See detailed info → Standardnear ASB7 · rs8027468
See detailed info → StandardLMX1B · rs10987373
See detailed info → Standardnear ABCA1 · rs2472496
See detailed info → StandardLOXL1 · rs1550437
See detailed info →Showing 20 of 444 · page 11 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.