8,154 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.
RIN3 · rs61975764
See detailed info → SensitiveHDAC9 · rs6950598
See detailed info → SensitiveSTK10 · rs9313579
See detailed info → SensitiveNRXN1 · rs4971775
See detailed info → SensitiveBMP7 · rs6014965
See detailed info → SensitiveSTK11 · rs62131228
See detailed info → SensitiveKLF14 · rs73161913
See detailed info → Sensitivenear SLC39A11 · rs983318
See detailed info → SensitiveSMAD9 · rs7333607
See detailed info → SensitiveMZF1 · rs73068325
See detailed info → SensitiveLRP1 · rs4759277
See detailed info → SensitiveSF3A3 · rs4360494
See detailed info → Sensitivenear KLF2 · rs34797592
See detailed info → SensitiveHHIP · rs11727676
See detailed info → SensitiveSLCO2A1 · rs10049390
See detailed info → SensitiveBOC · rs72942485
See detailed info → SensitiveSMAD3 · rs56324967
See detailed info → Sensitivenear TBRG4 · rs12672022
See detailed info → SensitiveCDH1 · rs9924886
See detailed info → SensitiveAPC · rs755229494
See detailed info →Showing 20 of 8154 · page 347 of 408
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.