28 positions on this site are linked to Central Corneal Thickness, out of 10,938 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
REEP3 · rs16920206
See detailed info → StandardTGFB2 · rs4846476
See detailed info → StandardLPAR1 · rs10980623
See detailed info → StandardCWC27 · rs1309531
See detailed info → StandardGLT8D2 · rs11111869
See detailed info → StandardGLT8D2 · rs11553764
See detailed info → StandardNT5DC3 · rs116878472
See detailed info → StandardLCN12 · rs7040970
See detailed info → StandardGLIS3 · rs7026684
See detailed info → StandardZNF469 · rs28687756
See detailed info → StandardADAMTS6 · rs10064391
See detailed info → StandardDCN · rs7308752
See detailed info → StandardARL4C · rs13024279
See detailed info → StandardSTON2 · rs56223983
See detailed info → StandardLOXL2 · rs3808520
See detailed info → StandardZNF469 · rs12448211
See detailed info → StandardARHGAP20 · rs4938174
See detailed info → StandardLPAR1 · rs1007000
See detailed info → StandardLCN12 · rs11145951
See detailed info → StandardTJP1 · rs785422
See detailed info →Showing 20 of 28 · page 1 of 2
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.