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.
SEMA3C/3D · rs80227144
See detailed info → StandardCYP2G1P · rs76935404
See detailed info → StandardCYP2G1P · rs10425738
See detailed info → StandardRAB4B-EGLN2 · rs11878604
See detailed info → StandardRAB4B-EGLN2 · rs2316205
See detailed info → StandardCYP2A6 · rs113029345
See detailed info → Standard on its ownCDH13 · rs12599112
See detailed info → StandardLZTFL1 · rs73064425
See detailed info → StandardINTS10 · rs7000921
See detailed info → SensitiveSLC6A13 · rs10774021
See detailed info → SensitiveCASC8 · rs4506170
See detailed info → SensitiveCASC19 · rs138042437
See detailed info → SensitiveMYEOV · rs12270641
See detailed info → SensitivePHTF2 · rs6465825
See detailed info → SensitivePRKAG2 · rs7805747
See detailed info → SensitiveSETDB1 · rs267734
See detailed info → Standard on its ownCENPW · rs139878170
See detailed info → Standard on its ownCCND1 · rs9344
See detailed info → Standard on its ownSMARCD3 · rs79419269
See detailed info → Standard on its ownPRTN3 · rs62132293
See detailed info →Showing 20 of 7431 · page 221 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.