7,772 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.
BCL2 · rs77551289
See detailed info → StandardPRKD2 · rs874460
See detailed info → StandardC6orf106 · rs3800461
See detailed info → StandardSP110 · rs34004493
See detailed info → StandardFARP2 · rs3755397
See detailed info → StandardLEF1 · rs7690934
See detailed info → StandardIRF4 · rs9392504
See detailed info → StandardPOT1 · rs2267708
See detailed info → StandardACTA · rs6586163
See detailed info → StandardC11orf21 · rs2651823
See detailed info → Standard on its ownRAPSN · rs12419342
See detailed info → StandardAS3MT · rs12416687
See detailed info → StandardACOXL · rs58055674
See detailed info → StandardLOC150577 · rs4851266
See detailed info → StandardAPOB · rs12713956
See detailed info → SensitiveDNAJC1 · rs11814448
See detailed info → Standard on its ownMAML3 · rs1531070
See detailed info → Standard on its ownCFH · rs800292
See detailed info → Sensitivenear GABBR1 · rs111508444
See detailed info → SensitivePDCD5 · rs12461589
See detailed info →Showing 20 of 7772 · page 258 of 389
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.