8,759 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.
EXOC3 · rs11739663
See detailed info → StandardIFNG · rs7134599
See detailed info → SensitiveTNPO · rs10488631
See detailed info → StandardDAP · rs267939
See detailed info → StandardLSP1 · rs907611
See detailed info → StandardCHRNA3 · rs1051730
See detailed info → StandardDBH · rs3025343
See detailed info → StandardBDNF · rs6265
See detailed info → SensitiveDUSP10 · rs6687758
See detailed info → SensitiveNOD2 · rs2076756
See detailed info → SensitiveIL23R · rs11209026
See detailed info → StandardUGT2A1 / UGT2A2 · rs7688383
See detailed info → StandardOR2M7 · rs4481887
See detailed info → StandardTAAR5 · rs41286168
See detailed info → Standard on its ownRBFOX3 · rs898534
See detailed info → StandardMC1R · rs12931267
See detailed info → SensitiveDUSP9 · rs5945326
See detailed info → SensitiveCENTD2 · rs1552224
See detailed info → SensitiveFTO · rs8050136
See detailed info → StandardZNF259 · rs964184
See detailed info →Showing 20 of 8759 · page 436 of 438
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.