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.
MMP16 · rs7819570
See detailed info → SensitiveCLU · rs73229090
See detailed info → SensitiveIMMP2L · rs13240464
See detailed info → SensitiveMLL5 · rs6466055
See detailed info → SensitiveGRM3 · rs12704290
See detailed info → SensitiveFUT9 · rs117074560
See detailed info → SensitiveRIMS1 · rs1339227
See detailed info → SensitiveGALNT10 · rs11740474
See detailed info → SensitiveGRIA1 · rs111294930
See detailed info → SensitiveMEF2C · rs16867576
See detailed info → SensitiveZSWIM6 · rs4391122
See detailed info → SensitiveMIR548AJ2 · rs215411
See detailed info → SensitiveCCDC39 · rs9841616
See detailed info → SensitiveTRANK1 · rs75968099
See detailed info → SensitiveC2orf82 · rs6704768
See detailed info → SensitivePCGEM1 · rs59979824
See detailed info → SensitiveKDM4A · rs11210892
See detailed info → Standard on its ownchr21q22 · rs2836883
See detailed info → SensitiveFANCL · rs11682175
See detailed info → SensitiveLRRIQ3 · rs12129573
See detailed info →Showing 20 of 12425 · page 519 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.