8,459 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.
PDE4B · rs1937443
See detailed info → Standard on its ownST6GALNAC3 · rs10873871
See detailed info → Standard on its ownnear NEGR1 · rs12740789
See detailed info → Standard on its ownnear CETP · rs17231520
See detailed info → StandardBTN1A1 · rs1056667
See detailed info → Standard on its ownABCB11 · rs557462
See detailed info → Standard on its ownPHC2 · rs10914684
See detailed info → Standard on its ownnear FOXO6 · rs12755632
See detailed info → Standard on its ownPTPRF · rs951740
See detailed info → Standard on its ownADGRB2 · rs1889571
See detailed info → Standard on its ownCAMTA1 · rs12130857
See detailed info → Standard on its ownnear HERPUD1 · rs56156922
See detailed info → Standard on its ownRRN3 · rs11644601
See detailed info → Standard on its ownALDH1A2 · rs7350789
See detailed info → Sensitive on its ownFADS1 · rs174562
See detailed info → Sensitive on its ownBTBD3 · rs686548
See detailed info → Sensitive on its ownACADS · rs34708625
See detailed info → Sensitive on its ownACADS · rs1799958
See detailed info → Sensitivenear CCDC68 · rs12966052
See detailed info → Sensitivenear EP300 · rs5995992
See detailed info →Showing 20 of 8459 · page 23 of 423
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.