10,866 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.
near DUSP10 · rs6658977
See detailed info → SensitiveFKBP5 · rs16878812
See detailed info → Sensitivenear SRSF3 · rs1321310
See detailed info → SensitiveBMP5 · rs62404966
See detailed info → Sensitivenear SLC25A28 · rs2193352
See detailed info → SensitivePOLD3 · rs57796856
See detailed info → Sensitivenear ATF1 · rs11169572
See detailed info → Sensitivenear STARD13 · rs9537521
See detailed info → SensitiveRHPN2 · rs73039434
See detailed info → SensitiveGATA3 · rs10795668
See detailed info → SensitiveL1TD1 · rs7542665
See detailed info → SensitiveEFCAB2 · rs201395236
See detailed info → SensitiveSLCO2A1 · rs113569514
See detailed info → SensitiveNOTCH4 · rs3830041
See detailed info → SensitiveDENND5B · rs77969132
See detailed info → SensitiveKLF5 · rs1886450
See detailed info → SensitiveMHC · rs116353863
See detailed info → SensitiveEIF3H · rs117079142
See detailed info → SensitiveSATB2 · rs11884596
See detailed info → SensitiveGREM1 · rs12708491
See detailed info →Showing 20 of 10866 · page 483 of 544
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.