7,431 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.
PADI4 · rs2301888
See detailed info → SensitiveAHNAK2 · rs2582532
See detailed info → SensitivePTPN2 · rs8083786
See detailed info → SensitiveRASGRP1 · rs8032939
See detailed info → SensitiveREL · rs34695944
See detailed info → SensitiveMTF1 · rs28411352
See detailed info → SensitiveLOC145837 · rs8026898
See detailed info → SensitiveLOC339442 · rs12140275
See detailed info → StandardPLG · rs4252129
See detailed info → Standard on its ownCDKN1A · rs1321313
See detailed info → StandardGLT25D2 · rs3814333
See detailed info → StandardSHROOM3 · rs10032549
See detailed info → Standard on its ownC6orf204 · rs6906287
See detailed info → Standard on its ownSLC41A1 · rs6679073
See detailed info → Standard on its ownKLK3 · rs2659051
See detailed info → StandardGSDMB · rs2305480
See detailed info → SensitiveTOX3 · rs12922061
See detailed info → SensitiveFAF1 · rs17106184
See detailed info → SensitiveTMEM154 · rs6813195
See detailed info → StandardNRG4 · rs11072566
See detailed info →Showing 20 of 7431 · page 277 of 372
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.