8,961 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.
FUT8 · rs11158592
See detailed info → SensitiveGABRR1 · rs9942471
See detailed info → StandardLMTK2 · rs34320230
See detailed info → Standardnear CSMD1 · rs13265017
See detailed info → Standardnear SEMA6D · rs1439321
See detailed info → Standardnear MEF2C · rs1644039
See detailed info → StandardGABBR1 · rs28986304
See detailed info → Standardnear ACVR2A · rs11686893
See detailed info → StandardFAM120A · rs10821129
See detailed info → StandardUBE2L6 · rs12364489
See detailed info → StandardVRK2 · rs60152647
See detailed info → StandardMSRA · rs7818437
See detailed info → StandardSGCZ · rs28639817
See detailed info → StandardMED24 · rs35982947
See detailed info → StandardBAIAP2 · rs56084168
See detailed info → StandardLINGO2 · rs12344656
See detailed info → StandardZDHHC5 · rs10896636
See detailed info → StandardMYO1H · rs11608355
See detailed info → StandardVPS41 · rs10274968
See detailed info → StandardANKRD10 · rs9521987
See detailed info →Showing 20 of 8961 · page 12 of 449
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.