9,513 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.
DRD2 · rs2514218
See detailed info → SensitiveSNX19 · rs10791097
See detailed info → SensitiveIGSF9B · rs75059851
See detailed info → SensitiveCACNA1C · rs2007044
See detailed info → SensitiveKDM4A · rs11210892
See detailed info → SensitiveFANCL · rs11682175
See detailed info → Standard on its ownchr21q22 · rs2836883
See detailed info → SensitiveANP32E · rs140505938
See detailed info → SensitiveLRRIQ3 · rs12129573
See detailed info → StandardPAX8 · rs1823125
See detailed info → Standard on its ownSVEP1 · rs7038415
See detailed info → Standard on its ownPTK2B · rs28834970
See detailed info → Standard on its ownIL12B · rs4379175
See detailed info → Standard on its ownIL17D · rs2253017
See detailed info → Standard on its ownchr13q21 · rs9540128
See detailed info → SensitiveTLE4 · rs17791513
See detailed info → Standardnear PRAG1 · rs2921036
See detailed info → StandardABCG2 · rs4148152
See detailed info → SensitiveTBC1D21 · rs16958445
See detailed info → Standardnear CSMD1 · rs2407746
See detailed info →Showing 20 of 9513 · page 374 of 476
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.