7,772 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.
HNF4A · rs1800961
See detailed info → StandardSALL1 · rs10521222
See detailed info → Standard on its ownNRTN · rs3760776
See detailed info → StandardGPR126 · rs4896582
See detailed info → StandardCD164 · rs9374080
See detailed info → StandardMARCH8 · rs11239550
See detailed info → SensitiveMAPT · rs393152
See detailed info → StandardRTBDN · rs7255045
See detailed info → Standard on its ownICAM-1 · rs3093030
See detailed info → StandardTHSD4 · rs12899618
See detailed info → Standard on its ownADIPOQ · rs1648707
See detailed info → StandardGCDH · rs11085824
See detailed info → StandardIL6 · rs2097677
See detailed info → SensitiveZFP36L2 · rs13429458
See detailed info → SensitiveDENND1A · rs10818854
See detailed info → Sensitivenear SMIM38 · rs7931342
See detailed info → StandardCFB · rs9380272
See detailed info → Standard on its ownnear PLXDC2 · rs12219125
See detailed info → StandardKCNJ2 · rs8079702
See detailed info → Standard on its ownARHGAP1 · rs7932354
See detailed info →Showing 20 of 7772 · page 355 of 389
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.