7,839 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.
LOC100130673 · rs17161076
See detailed info → Standard on its ownINO80D · rs972540
See detailed info → Standard on its ownPRDX1 · rs2275426
See detailed info → Standard on its ownREG3G · rs17016673
See detailed info → Standard on its ownPOU3F3 · rs1451533
See detailed info → Standard on its ownSMG6 · rs9914578
See detailed info → Standard on its ownAGBL4 · rs3127553
See detailed info → Standard on its ownAGBL4 · rs657452
See detailed info → Standard on its ownCCL3 · rs12150665
See detailed info → Standard on its ownGOLGA5 · rs3783890
See detailed info → Standard on its ownnear MCTP2 · rs7181659
See detailed info → Standard on its ownRPH3A · rs729062
See detailed info → Standard on its ownSFSWAP · rs11247009
See detailed info → Standard on its ownNSF · rs11652097
See detailed info → Standard on its ownUGGT2 · rs9634489
See detailed info → Standard on its ownDDX11L10 · rs11866815
See detailed info → Standard on its ownURI1 · rs33439
See detailed info → Standard on its ownKCNJ18 · rs4986044
See detailed info → Standard on its ownCNTN1 · rs1405552
See detailed info → Standard on its ownKCNJ16 · rs312750
See detailed info →Showing 20 of 7839 · page 35 of 392
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.