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.
TNFRSF13B · rs4985726
See detailed info → SensitiveACAD10 · rs11066015
See detailed info → StandardGUCY1A3 · rs13139571
See detailed info → StandardKPNA4 · rs17236529
See detailed info → StandardC5orf23 · rs1173771
See detailed info → Standard on its ownTNFRSF13B · rs4561508
See detailed info → StandardTBL2 · rs2286276
See detailed info → StandardADCY3 · rs11676272
See detailed info → StandardKLKB1 · rs4253252
See detailed info → StandardPRODH · rs2023634
See detailed info → StandardLCAT · rs16942887
See detailed info → Standard on its ownHBB · rs12788102
See detailed info → StandardPDXDC1 · rs7200543
See detailed info → SensitiveSLC22A1 · rs651164
See detailed info → StandardC12orf51 · rs2074356
See detailed info → Standard on its ownABO · rs8176722
See detailed info → StandardDCDC5 · rs10767873
See detailed info → SensitiveTSHR · rs12101261
See detailed info → SensitiveJAZF1 · rs849134
See detailed info → StandardST3GAL4 · rs11220462
See detailed info →Showing 20 of 12481 · page 556 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.