8,381 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.
KLF5 · rs17285550
See detailed info → StandardRORA · rs76194223
See detailed info → StandardAP4E1 · rs11634895
See detailed info → SensitiveAPOE · rs429358
See detailed info → Standard on its ownPHB2 · rs2110073
See detailed info → Standard on its ownMBOAT5 · rs12580543
See detailed info → Standard on its ownEXOG · rs7433306
See detailed info → Standard on its ownPRDM16 · rs2483280
See detailed info → Standard on its ownHLA · rs12195582
See detailed info → Standard on its ownETS1 · rs4937362
See detailed info → Standard on its ownBCL2 · rs17749561
See detailed info → Standard on its ownPVT1 · rs13254990
See detailed info → Standard on its ownSIK3 · rs681524
See detailed info → Standard on its ownISL1 · rs9291768
See detailed info → SensitiveC2 · rs558702
See detailed info → Standard on its ownMYC · rs13255292
See detailed info → Standard on its ownABO · rs8176749
See detailed info → Standard on its ownMYC · rs4733601
See detailed info → SensitiveTP63 · rs13314271
See detailed info → SensitiveFAM98B · rs11073328
See detailed info →Showing 20 of 8381 · page 305 of 420
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.