8,284 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.
PMSP · rs115146037
See detailed info → SensitiveC3orf70 · rs7647854
See detailed info → Standard on its ownDDX39B · rs114050967
See detailed info → Standard on its ownMICB · rs3130614
See detailed info → Standard on its ownHCP5 · rs115902351
See detailed info → Standard on its ownHCG26 · rs114771815
See detailed info → Standard on its ownHCG26 · rs116088953
See detailed info → SensitiveHLA-B · rs1050529
See detailed info → SensitiveTNS3 · rs7776701
See detailed info → SensitiveOBFC1 · rs7907606
See detailed info → SensitiveZFHX4 · rs10093547
See detailed info → SensitiveGATA3 · rs73635312
See detailed info → SensitiveRHOU · rs61824911
See detailed info → SensitiveOCA2 · rs12916300
See detailed info → SensitiveZBTB10 · rs11993814
See detailed info → SensitiveCUX1 · rs73183643
See detailed info → SensitiveFOXP1 · rs2116709
See detailed info → SensitiveRGS22 · rs141115006
See detailed info → Standard on its ownSELP · rs6703865
See detailed info → StandardZNF652 · rs12940887
See detailed info →Showing 20 of 8284 · page 246 of 415
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.