7,431 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.
F12 · rs2731672
See detailed info → Standard on its ownEDN1 · rs5370
See detailed info → StandardIGF2BP3 · rs12534093
See detailed info → StandardC3orf47 · rs6439167
See detailed info → StandardOR2J3 · rs3129109
See detailed info → Standard on its ownPEPD · rs4805885
See detailed info → SensitiveLRFN2 · rs2494938
See detailed info → Standard on its ownIGHG1 · rs10136766
See detailed info → StandardIL7R · rs6890853
See detailed info → SensitiveLILRA3 · rs103294
See detailed info → Standard on its ownMAG13 · rs1230666
See detailed info → StandardRUNX1 · rs150498232
See detailed info → StandardC20orf203 · rs6058796
See detailed info → SensitiveNDST3 · rs11098403
See detailed info → StandardCA5A · rs8056952
See detailed info → StandardZFPM1 · rs12447180
See detailed info → StandardVMP1 · rs1292061
See detailed info → StandardPRTN3 · rs56757486
See detailed info → StandardFUT6 · rs778798
See detailed info → SensitiveSALM1 · rs34517613
See detailed info →Showing 20 of 7431 · page 278 of 372
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.