7,860 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
PLXNC1 · rs61708525
See detailed info → SensitiveNCF4 · rs760517
See detailed info → SensitivePRDX5 · rs11231749
See detailed info → SensitiveSPRED2 · rs13385171
See detailed info → SensitiveTHEMIS · rs802730
See detailed info → SensitiveCSF2RB · rs5756405
See detailed info → SensitiveEPPK1 · rs3923387
See detailed info → SensitiveLOC101929282 · rs962052
See detailed info → SensitiveB4GALT5 · rs6020055
See detailed info → SensitiveSMARCA4 · rs12609500
See detailed info → SensitiveIL2RA · rs12253981
See detailed info → SensitiveGALC · rs74796499
See detailed info → SensitiveZFP36L1 · rs2236262
See detailed info → SensitiveTSFM · rs201202118
See detailed info → SensitiveCD69 · rs11052877
See detailed info → Sensitivenear TTC33 · rs6880778
See detailed info → SensitiveC1orf106 · rs55838263
See detailed info → SensitiveSLC2A4RG · rs2256814
See detailed info → SensitiveSLC9A8 · rs17785991
See detailed info → SensitiveMIR548AN · rs4772201
See detailed info →Showing 20 of 7860 · page 257 of 393
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.