12,444 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.
LINC00506 · rs17023900
See detailed info → StandardRREB1 · rs675209
See detailed info → Standard on its ownKIAA0825 · rs17376456
See detailed info → Standard on its ownAHR · rs6968865
See detailed info → StandardBCL11A · rs11886868
See detailed info → Sensitivenear VGLL3 · rs2660753
See detailed info → SensitiveSLC22A3 · rs9364554
See detailed info → SensitivePOU5F1B · rs6983267
See detailed info → SensitiveITGAM · rs9888739
See detailed info → StandardTMCC2 · rs1668873
See detailed info → StandardHLA-C · rs12191877
See detailed info → StandardTNIP1 · rs17728338
See detailed info → StandardGATA2 · rs4857855
See detailed info → SensitiveWDR12 · rs6725887
See detailed info → Standard on its ownATP10D · rs10938494
See detailed info → StandardCHRNA3 / CHRNA5 · rs8042849
See detailed info → StandardFURIN / FES · rs6224
See detailed info → StandardATXN2 / BRAP · rs11065979
See detailed info → StandardCDKN2B-AS1 · rs1556516
See detailed info → StandardLPA · rs10455872
See detailed info →Showing 20 of 12444 · page 591 of 623
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.