12,426 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.
VEGFA · rs11755845
See detailed info → Standardnear OR51V1 · rs7120391
See detailed info → StandardCAPZB · rs10799824
See detailed info → StandardVEGFA · rs9472138
See detailed info → StandardRDHE2 · rs4075154
See detailed info → StandardLPA · rs186696265
See detailed info → StandardMAFB · rs1883711
See detailed info → StandardPPP1R3B · rs2169387
See detailed info → StandardSNX5 · rs2618568
See detailed info → StandardPPARG · rs2920503
See detailed info → StandardST3GAL4 · rs4307732
See detailed info → Standard on its ownSORBS2 · rs4862562
See detailed info → StandardCILP2 · rs73001065
See detailed info → StandardGRINA · rs11784833
See detailed info → StandardNYNRIN · rs11621792
See detailed info → StandardFAM117B · rs140244541
See detailed info → SensitiveG6PD · rs1050829
See detailed info → SensitiveMT-RNR1 · rs267606617
See detailed info → SensitiveRYR1 · rs118192172
See detailed info → StandardVIP · rs9479402
See detailed info →Showing 20 of 12426 · page 500 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.