12,481 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.
CADPS · rs76824303
See detailed info → StandardFIGN · rs80163246
See detailed info → StandardSLC4A10 · rs62189006
See detailed info → StandardFSHR · rs13023587
See detailed info → StandardFANCL · rs17049683
See detailed info → StandardLINC01793 · rs11125776
See detailed info → SensitiveNT5C2 · rs11191580
See detailed info → StandardPREPL · rs9309116
See detailed info → StandardPRRC2C · rs35039375
See detailed info → StandardFAM23A · rs2477664
See detailed info → StandardPARVB · rs2896019
See detailed info → StandardALPL · rs2242420
See detailed info → StandardADM · rs7129220
See detailed info → StandardRWDD3 · rs2893323
See detailed info → StandardFNDC5 · rs2786547
See detailed info → SensitivePCSK7 · rs508487
See detailed info → SensitiveSLC17A4 · rs11754288
See detailed info → StandardDKK1 · rs1733724
See detailed info → StandardFGG · rs7681423
See detailed info → Standard on its ownHMGA2 · rs10784502
See detailed info →Showing 20 of 12481 · page 560 of 625
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.