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.
BRCA2 · rs11571833
See detailed info → SensitiveFRY · rs56084662
See detailed info → SensitiveBABAM1 · rs4808075
See detailed info → SensitiveRAD51B · rs11844632
See detailed info → SensitiveNOS1 · rs73208120
See detailed info → SensitiveSLC25A26 · rs812481
See detailed info → SensitiveCTNNB1 · rs35360328
See detailed info → SensitiveENTPD7 · rs11190164
See detailed info → SensitiveGREM1 · rs2293582
See detailed info → SensitiveVTI1A · rs12241008
See detailed info → SensitiveLAMA5 · rs2427308
See detailed info → SensitiveDIP2B · rs34245511
See detailed info → SensitiveSLC25A28 · rs1035209
See detailed info → SensitiveRHPN2 · rs10411210
See detailed info → SensitivePOU2AF3 · rs3802842
See detailed info → SensitiveTGFB1 · rs1800469
See detailed info → SensitiveAS1 · rs704017
See detailed info → SensitivePLCB1 · rs2423279
See detailed info → SensitiveNABP1 · rs11903757
See detailed info → StandardAKR1C4 · rs182498797
See detailed info →Showing 20 of 10866 · page 487 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.