12,481 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.
CPEB4 · rs6861681
See detailed info → StandardFAM120B · rs9460110
See detailed info → StandardSCAF8 · rs140506252
See detailed info → StandardPRDM13 · rs9389556
See detailed info → StandardKCTD16 · rs10875606
See detailed info → StandardZSCAN9 · rs11967137
See detailed info → StandardSTK32A · rs10875622
See detailed info → StandardEFNA5 · rs388016
See detailed info → StandardPAM · rs2195272
See detailed info → StandardFLJ45244 · rs8014194
See detailed info → SensitiveTCN2 · rs2283873
See detailed info → SensitiveNHS · rs5955543
See detailed info → Standard on its ownnear MUC22 · rs9262632
See detailed info → StandardGBE1 · rs9883093
See detailed info → SensitiveMYCN · rs3755132
See detailed info → StandardPRKD1 · rs11847697
See detailed info → StandardTNNI3K · rs1514175
See detailed info → StandardPGM1 · rs2749097
See detailed info → StandardZBTB38 · rs6440003
See detailed info → StandardKLHL29 · rs13033444
See detailed info →Showing 20 of 12481 · page 559 of 625
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.