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.
CHD9 · rs11859517
See detailed info → StandardPLEC · rs11780978
See detailed info → StandardCAPN3 · rs56702977
See detailed info → StandardPSMG1 · rs9808651
See detailed info → StandardSPPL2A · rs12913259
See detailed info → Standard on its ownIPP · rs61784824
See detailed info → Standard on its ownMYRF · rs174528
See detailed info → Standard on its ownFADS2 · rs174577
See detailed info → StandardMIR2392 · rs6575803
See detailed info → StandardSPRED1 · rs75844534
See detailed info → StandardASPSCR1 · rs9912553
See detailed info → StandardDCST2 · rs6426985
See detailed info → StandardFAM46C · rs41276588
See detailed info → StandardAGTR2 · rs6608539
See detailed info → Standardnear HLA-DQB1 · rs1794280
See detailed info → StandardBCAR1 · rs11641308
See detailed info → StandardLINC00485 · rs2647873
See detailed info → StandardCHMP4B · rs181451002
See detailed info → StandardITPR2 · rs2306547
See detailed info → StandardAPOLD1 · rs11055030
See detailed info →Showing 20 of 7772 · page 228 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.