8,177 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.
BCAR1 · rs11641308
See detailed info → StandardLINC00485 · rs2647873
See detailed info → StandardCHMP4B · rs181451002
See detailed info → StandardITPR2 · rs2306547
See detailed info → StandardAPOLD1 · rs11055030
See detailed info → StandardANO1 · rs61885091
See detailed info → StandardWT1 · rs5030317
See detailed info → StandardADM · rs4444073
See detailed info → StandardKCNQ1 · rs234864
See detailed info → StandardSOCS5 · rs7596521
See detailed info → StandardABLIM3 · rs9687065
See detailed info → Standard on its ownCHRNA3 · rs138544659
See detailed info → Standard on its ownGRIN3A · rs10989692
See detailed info → SensitiveTP63 · rs9854771
See detailed info → SensitiveSUGCT · rs17688601
See detailed info → SensitiveHDAC9 · rs11984041
See detailed info → SensitiveABCC1 · rs74475935
See detailed info → SensitiveTSPAN2 · rs12122341
See detailed info → StandardFAM3A · rs5030868
See detailed info → StandardNPRL3 · rs570013781
See detailed info →Showing 20 of 8177 · page 249 of 409
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.