7,519 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.
INPP5E · rs10781499
See detailed info → StandardTNPO3 · rs4728142
See detailed info → StandardIL7R · rs3194051
See detailed info → StandardIL10 · rs3024505
See detailed info → StandardHLA-DRA · rs9268923
See detailed info → StandardNOTCH4 · rs549182
See detailed info → StandardC1orf106 · rs7554511
See detailed info → StandardIFNG · rs1558744
See detailed info → StandardHLA · rs9263739
See detailed info → SensitiveLRRK2 · rs17466626
See detailed info → SensitiveSUOX · rs1689510
See detailed info → SensitiveNOD2 · 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 →Showing 20 of 7519 · page 357 of 376
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.