95 positions on this site are linked to Myopia, out of 9,215 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near NRIP1 · rs2823141
See detailed info → StandardSLC25A12 · rs72890842
See detailed info → StandardGNB3 · rs5442
See detailed info → StandardCDH13 · rs80124906
See detailed info → StandardTMEM98 · rs62067167
See detailed info → StandardDSCAML1 · rs715315
See detailed info → StandardGAS6 · rs6602906
See detailed info → StandardMYO5B · rs12965607
See detailed info → Standardnear GK2 · rs7662551
See detailed info → StandardNFIA · rs479445
See detailed info → Standardnear ZNF281 · rs10919908
See detailed info → StandardTIAM1 · rs7275394
See detailed info → Standardnear ZNF519 · rs11872104
See detailed info → Standardnear H2BC11 · rs13217285
See detailed info → Standardnear FAM240C · rs12998513
See detailed info → Standardnear HAPSTR2 · rs7067005
See detailed info → StandardRDH5 · rs3138141
See detailed info → StandardDPP6 · rs12667032
See detailed info → StandardTRIM25 · rs28488643
See detailed info → StandardPDE11A · rs17400325
See detailed info →Showing 20 of 95 · page 4 of 5
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.