12,469 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.
CCDC26 · rs891835
See detailed info → StandardCRP · rs7553007
See detailed info → StandardHHIP · rs13147758
See detailed info → StandardPLN · rs11970286
See detailed info → StandardLITAF · rs8049607
See detailed info → StandardIL6R · rs4537545
See detailed info → StandardGLUT9 · rs6855911
See detailed info → SensitiveUBE4B · rs17401966
See detailed info → StandardHLA-B · rs2523590
See detailed info → StandardNCAN · rs16996148
See detailed info → StandardSLC7A9 · rs8101881
See detailed info → StandardGSTCD · rs10516526
See detailed info → StandardHHIP · rs12504628
See detailed info → Standard on its ownPDGFC · rs4234898
See detailed info → StandardHHIP · rs1492820
See detailed info → StandardHIST1H1D · rs10946808
See detailed info → SensitiveADM · rs6484218
See detailed info → StandardHNF4A · rs1800961
See detailed info → StandardSALL1 · rs10521222
See detailed info → Standard on its ownNRTN · rs3760776
See detailed info →Showing 20 of 12469 · page 589 of 624
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.