8,838 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.
DGKK · rs4554617
See detailed info → SensitiveTANC1 · rs7582141
See detailed info → StandardCETP · rs118146573
See detailed info → StandardSIK3 · rs11216230
See detailed info → StandardTAX1BP1 · rs10214930
See detailed info → StandardHOXA4 · rs1801085
See detailed info → StandardPDGFC · rs13124827
See detailed info → StandardEEFSEC · rs2999052
See detailed info → StandardHAAO · rs3816183
See detailed info → StandardPKDCC · rs988958
See detailed info → SensitiveURAD · rs9581943
See detailed info → StandardZFHX3 · rs1858800
See detailed info → StandardKCNMA1 · rs10762738
See detailed info → StandardCCDC26 · rs17262815
See detailed info → StandardIGFBP3 · rs7811653
See detailed info → Standard on its ownIL13 · rs2069757
See detailed info → Standard on its ownCAPN14 · rs149864795
See detailed info → Standard on its ownCAV1 · rs10258482
See detailed info → StandardMAP4K2 · rs10897526
See detailed info → Standardnear ZNF518B · rs79824542
See detailed info →Showing 20 of 8838 · page 333 of 442
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.