8,812 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.
RARRES1 · rs9849301
See detailed info → StandardFYN · rs2012071
See detailed info → StandardPIP5K1B · rs7042283
See detailed info → Sensitive on its ownS100A10 · rs6587640
See detailed info → Sensitive on its ownMMP20 · rs1317947
See detailed info → SensitiveSLC1A1 · rs1471786
See detailed info → Sensitive on its ownKIRREL2 · rs447707
See detailed info → Standard on its ownnear DEF8 · rs4785752
See detailed info → Sensitive on its ownZFP64 · rs6022039
See detailed info → SensitiveMEGF10 · rs72790443
See detailed info → Standard on its ownRALGPS1 · rs3739555
See detailed info → Standard on its ownTGFB2 · rs17047703
See detailed info → Standard on its ownDNALI1 · rs2268695
See detailed info → Standard on its ownSAMMSON · rs34552401
See detailed info → Standard on its ownRNF166 · rs75410747
See detailed info → Standard on its ownnear CDH15 · rs117156175
See detailed info → Standard on its ownVPS9D1 · rs57119673
See detailed info → Standard on its ownANKRD11 · rs55637757
See detailed info → Standard on its ownSTAG1 · rs13092193
See detailed info → Standard on its ownCDO1 · rs34869
See detailed info →Showing 20 of 8812 · page 16 of 441
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.