12,428 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.
NOD2 · rs117372389
See detailed info → SensitiveFUT2 · rs602662
See detailed info → SensitivePSMG1 · rs2836882
See detailed info → StandardC6orf10 · rs2395185
See detailed info → StandardPSMG1 · rs2836878
See detailed info → StandardNKX2-3 · rs11190140
See detailed info → StandardPUS10 · rs13003464
See detailed info → SensitiveTNFSF15 · rs2006996
See detailed info → StandardCALM3 · rs1126510
See detailed info → StandardITPKA · rs28374715
See detailed info → StandardMAML2 · rs483905
See detailed info → SensitiveANKRD30A · rs7100025
See detailed info → SensitiveDAG1 · rs4625
See detailed info → SensitivePTGER4 · rs7725052
See detailed info → SensitiveIL5 · rs11741255
See detailed info → SensitiveADCY7 · rs77150043
See detailed info → SensitiveZMIZ1 · rs1250563
See detailed info → StandardSTX7 · rs4470875
See detailed info → StandardCYP2C19 · rs35013847
See detailed info → StandardNOS1AP · rs12567315
See detailed info →Showing 20 of 12428 · page 603 of 622
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.