8,057 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.
CHRNB4 · rs11639372
See detailed info → Standardnear GYPA · rs17766287
See detailed info → Standardnear HHIP · rs1490151
See detailed info → StandardPSMA4 · rs3813570
See detailed info → StandardAGPHD1 · rs12439240
See detailed info → Standardnear GYPA · rs4835177
See detailed info → StandardFAM13A · rs7682317
See detailed info → StandardCHRNB4 · rs12441088
See detailed info → Standardnear HHIP · rs35937742
See detailed info → StandardRAPSN · rs7103648
See detailed info → StandardFGD5 · rs11128722
See detailed info → StandardDBH · rs6271
See detailed info → StandardCSNK1G3 · rs6891344
See detailed info → StandardGNAS · rs6026748
See detailed info → StandardADRB1 · rs740746
See detailed info → StandardSYNPO2L · rs12247028
See detailed info → StandardC10orf107 · rs7076398
See detailed info → StandardBLK · rs2898290
See detailed info → StandardPIK3C · rs12705390
See detailed info → Standard on its ownGLI3 · rs17640804
See detailed info →Showing 20 of 8057 · page 237 of 403
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.