7,972 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.
LPL · rs10105606
See detailed info → Standard on its ownLDLR · rs6511720
See detailed info → Standard on its ownCELSR2 · rs7528419
See detailed info → StandardNCAN · rs17216525
See detailed info → SensitiveGATA3 · rs11255841
See detailed info → StandardF3 · rs12029080
See detailed info → Standard on its ownATOH7 · rs1900004
See detailed info → StandardRAP1A · rs494453
See detailed info → StandardC2orf16 · rs1919128
See detailed info → StandardLPA · rs1084651
See detailed info → StandardALDH1A2 · rs493258
See detailed info → StandardSBNO1 · rs4759375
See detailed info → StandardUBE2L3 · rs181362
See detailed info → StandardCITED2 · rs605066
See detailed info → StandardANGPTL4 · rs7255436
See detailed info → StandardPPP6R3 · rs12283755
See detailed info → Standard on its ownFRAP1 · rs17036350
See detailed info → Standard on its ownPDGFRA · rs2114039
See detailed info → Standard on its ownTRIM47 · rs1055129
See detailed info → StandardCD80 · rs2293370
See detailed info →Showing 20 of 7972 · page 352 of 399
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.