9,043 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.
RASSF1 · rs2073498
See detailed info → Standard on its ownNTM · rs10750486
See detailed info → StandardLOC105377005 · rs2643826
See detailed info → StandardNPR3 · rs3762988
See detailed info → StandardRPP25 · rs34063670
See detailed info → Standard on its ownGRM8 · rs3808072
See detailed info → Standard on its ownnear CELF4 · rs72893199
See detailed info → Standard on its ownPALM · rs116962250
See detailed info → Standard on its ownECE1 · rs7543687
See detailed info → Standard on its ownCRB1 · rs2488398
See detailed info → Standard on its ownDSCAM · rs2205129
See detailed info → Standard on its ownB3GALT1 · rs1375311
See detailed info → Standard on its ownMCHR1 · rs13054099
See detailed info → Standard on its ownMYO1H · rs7132057
See detailed info → Standard on its ownNCOA6 · rs62213709
See detailed info → Standard on its ownBBX · rs1697692
See detailed info → Standard on its ownHIVEP1 · rs9462364
See detailed info → Standard on its ownGOSR2 · rs1378358
See detailed info → Standard on its ownTAC1 · rs6948180
See detailed info → Standard on its ownNF1 · rs17884466
See detailed info →Showing 20 of 9043 · page 11 of 453
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.