7,939 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.
USP50 · rs3105593
See detailed info → StandardKLF12 · rs728926
See detailed info → StandardATP2A2 · rs3026445
See detailed info → StandardFADS2 · rs174583
See detailed info → Standard on its ownMED13 · rs10850409
See detailed info → Standard on its ownEFHA1 · rs2798269
See detailed info → StandardFBXL13 · rs17135875
See detailed info → SensitiveBTBD8 · rs34856868
See detailed info → StandardRNF114 · rs1056198
See detailed info → StandardIL23R · rs9988642
See detailed info → StandardPOL1 · rs545979
See detailed info → StandardPTRF · rs963986
See detailed info → StandardPRM3 · rs367569
See detailed info → StandardEXOC2 · rs9504361
See detailed info → StandardSLC45A1 · rs11121129
See detailed info → StandardPRSS53 · rs12445568
See detailed info → StandardSTAT2 · rs2066819
See detailed info → StandardKLF13 · rs28624578
See detailed info → StandardUBAC2 · rs9513593
See detailed info → StandardCHUK · rs61871342
See detailed info →Showing 20 of 7939 · page 256 of 397
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.