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.
ISL1 · 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 → SensitiveEDEM3 · rs10911628
See detailed info → StandardSCN1A · rs6732655
See detailed info → Standard on its ownMDM2 · rs73329476
See detailed info → Standard on its ownCCDC91 · rs1979679
See detailed info → Standard on its ownLOC100506393 · rs11045000
See detailed info → Standard on its ownRSPO2 · rs374810
See detailed info → Standard on its ownLOC283710 · rs8041227
See detailed info → Standard on its ownTREH · rs507080
See detailed info → Standard on its ownEXOC2 · rs116446171
See detailed info → Standard on its ownNCOA1 · rs79480871
See detailed info → StandardMMP8 · rs1939012
See detailed info → StandardPCDH7 · rs28498976
See detailed info → Standard on its ownAGXT2 · rs40200
See detailed info →Showing 20 of 8408 · page 307 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.