8,408 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.
FLI1 · rs10790969
See detailed info → Standard on its ownnear MOGAT2 · rs600518
See detailed info → StandardGIPR · rs34783010
See detailed info → Standardnear DCDC1 · rs55733296
See detailed info → Standard on its ownMADD · rs10838692
See detailed info → Standard on its ownMYRF · rs174529
See detailed info → Standard on its ownGPAM · rs7096937
See detailed info → Standard on its ownGPAM · rs77147124
See detailed info → Standard on its ownGPAM · rs2803621
See detailed info → Standard on its ownABCA1 · rs11789603
See detailed info → Standard on its ownABCA1 · rs12686004
See detailed info → Standard on its ownABCA1 · rs2740488
See detailed info → Standard on its ownMARCHF8 · rs11239549
See detailed info → Standard on its ownABCA1 · rs3847302
See detailed info → Standard on its ownnear LPL · rs79236614
See detailed info → Standard on its ownnear LPL · rs34770253
See detailed info → Standard on its ownnear LPL · rs28526159
See detailed info → Standard on its ownnear LPL · rs17489282
See detailed info → Standard on its ownnear SLC18A1 · rs6999158
See detailed info → Standard on its ownMROH8 · rs73094911
See detailed info →Showing 20 of 8408 · page 25 of 421
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.