12,425 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.
COL5A1 · rs1536482
See detailed info → StandardADAMTS6 · rs2307121
See detailed info → SensitiveADAM29 · rs6828523
See detailed info → StandardGLT8D2 · rs1564892
See detailed info → StandardARHGAP20 · rs4938174
See detailed info → StandardLCN12 · rs11145951
See detailed info → Standard on its ownFURIN · rs6227
See detailed info → Standard on its ownDARC · rs13962
See detailed info → StandardCERS3 · rs80332023
See detailed info → StandardCYP17A1 · rs4409766
See detailed info → StandardGUCY1A3 · rs13143871
See detailed info → StandardFGF5 · rs1902859
See detailed info → StandardCYP21A2 · rs2021783
See detailed info → StandardCACNA1D · rs9810888
See detailed info → Standardnear DPT · rs7518687
See detailed info → StandardCASC15 · rs10484389
See detailed info → StandardARID5B · rs4245595
See detailed info → StandardKCNH5 · rs76513344
See detailed info → Standard7SK · rs60283548
See detailed info → StandardKLF4 · rs60634637
See detailed info →Showing 20 of 12425 · page 522 of 622
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.