12,469 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.
CDKAL1 · rs9356744
See detailed info → SensitiveSCARB2 · rs6812193
See detailed info → SensitiveEXOC2 · rs12210050
See detailed info → Sensitive on its ownF11 · rs2289252
See detailed info → Sensitive on its ownSELP · rs6028
See detailed info → StandardTRIB1 · rs2980879
See detailed info → StandardTARDBP · rs12565727
See detailed info → SensitiveSLC30A8 · rs3802177
See detailed info → StandardDNAH10 · rs6488898
See detailed info → StandardADIPOQ · rs182052
See detailed info → StandardDGKK · rs1934179
See detailed info → StandardCSNK2A2 · rs74019828
See detailed info → SensitiveGPR183 · rs9557195
See detailed info → StandardZNF259 · rs11823543
See detailed info → StandardTRIB1 · rs2954033
See detailed info → SensitiveLPL · rs301
See detailed info → Standard on its ownDISC1 · rs12042938
See detailed info → StandardKLHDC8B · rs7617480
See detailed info → StandardIKZF2 · rs12619285
See detailed info → StandardNEDD8 · rs11158609
See detailed info →Showing 20 of 12469 · page 580 of 624
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.