12,479 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.
BOC · 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 → SensitivePITX1 · rs4976270
See detailed info → SensitivePNKD · rs3731861
See detailed info → SensitiveCTNNB1 · rs35470271
See detailed info → SensitiveRHPN2 · rs28840750
See detailed info → SensitiveMYRF · rs174533
See detailed info → SensitiveDUSP10 · rs17011141
See detailed info → SensitiveA1CF · rs10821907
See detailed info → SensitiveCCND2 · rs35808169
See detailed info → SensitiveLINC00603 · rs12514517
See detailed info → SensitiveHAO1 · rs11087784
See detailed info → SensitiveDACT1 · rs8020436
See detailed info → SensitiveNXN · rs73975586
See detailed info → SensitiveEIF3H · rs6469654
See detailed info → SensitiveBMP4 · rs4901473
See detailed info → SensitiveGREM1 · rs12708491
See detailed info →Showing 20 of 12479 · page 564 of 624
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.