7,972 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.
EBF2 · rs6991952
See detailed info → Standard on its ownADAMTS6 · rs370763
See detailed info → Standard on its ownEN1 · rs115242848
See detailed info → Standard on its ownSOST · rs71382995
See detailed info → StandardACTN1 · rs117672662
See detailed info → Standard on its ownRSPO3 · rs577721086
See detailed info → Standard on its ownMYRF · rs509360
See detailed info → Standard on its ownSLC6A15 · rs993226
See detailed info → StandardHLA-DQB1 · rs2856718
See detailed info → Standardc6orf10 · rs41268896
See detailed info → Sensitive on its ownLOC100505718 · rs16935279
See detailed info → StandardUBR1 · rs62020698
See detailed info → StandardMLXIPL · rs9638182
See detailed info → StandardLPA · rs7759633
See detailed info → StandardRSPO3 · rs72959041
See detailed info → StandardLRP1 · rs61352607
See detailed info → Standard on its ownJAK2 · rs12339666
See detailed info → StandardANGPTL3 · rs9988450
See detailed info → Standard on its ownADAMTS13 · rs3118667
See detailed info → StandardCRIM1 · rs3755206
See detailed info →Showing 20 of 7972 · page 255 of 399
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.