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.
NCOA7 · rs11154334
See detailed info → Standardnear FGF9 · rs9506725
See detailed info → StandardCDKL1 · rs72677850
See detailed info → StandardPHTF2 · rs7796089
See detailed info → StandardBANK1 · rs17248480
See detailed info → StandardGIP · rs35895680
See detailed info → StandardWHSC1L1 · rs11785041
See detailed info → StandardCREB3L1 · rs72910063
See detailed info → StandardPPM1E · rs34556895
See detailed info → StandardAKAP13 · rs12909648
See detailed info → Standard on its ownWRN · rs118130881
See detailed info → Standard on its ownDAB1 · rs74834332
See detailed info → SensitivePAX5 · rs7030813
See detailed info → Standard on its ownnear GRM5 · rs7937452
See detailed info → Standard on its ownDBNDD1 · rs77733403
See detailed info → Standard on its ownEXOC2 · rs71550013
See detailed info → SensitiveDENND1A · rs2670139
See detailed info → Standard on its ownnear SMIM38 · rs72932540
See detailed info → Standard on its ownPDE4B · rs1308048
See detailed info → Standard on its ownTRPS1 · rs2737212
See detailed info →Showing 20 of 8759 · page 19 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.