7,772 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.
RNF213 · rs9907978
See detailed info → Sensitive on its ownTCN2 · rs117353193
See detailed info → Sensitive on its ownRNF213 · rs10782008
See detailed info → Sensitive on its ownHORMAD2 · rs9614159
See detailed info → Sensitive on its ownMAGI2 · rs74388387
See detailed info → SensitiveIRS1 · rs2943656
See detailed info → SensitiveJAZF1 · rs1708302
See detailed info → SensitiveIGF2BP2 · rs71320321
See detailed info → SensitiveMHC · rs115918645
See detailed info → SensitiveCDC25A · rs7617773
See detailed info → Sensitivenear NGF · rs11806316
See detailed info → SensitiveTSPAN14 · rs17680741
See detailed info → SensitiveMAD1L1 · rs10267593
See detailed info → SensitivePCIF1 · rs3827066
See detailed info → SensitiveDAB2IP · rs885150
See detailed info → Sensitivenear TENT5A · rs4613862
See detailed info → SensitiveHTRA1 · rs4752700
See detailed info → SensitiveKIAA1462 · rs9337951
See detailed info → SensitiveTEX41 · rs7604735
See detailed info → SensitiveMIR6890 · rs73082363
See detailed info →Showing 20 of 7772 · page 36 of 389
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.