8,459 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.
near EP300 · rs5995992
See detailed info → SensitivePCDH9 · rs9592461
See detailed info → SensitivePIPOX · rs75581564
See detailed info → SensitiveSHANK2 · rs7117514
See detailed info → Sensitivenear KIRREL3 · rs57344483
See detailed info → SensitiveSPPL3 · rs3213572
See detailed info → Sensitivenear OLFM4 · rs1343605
See detailed info → SensitiveSTK24 · rs4772087
See detailed info → SensitiveDAGLA · rs198457
See detailed info → SensitivePIK3AP1 · rs1023741
See detailed info → SensitiveBRINP3 · rs10920654
See detailed info → Sensitivenear MEIS2 · rs8037355
See detailed info → Sensitivenear CMPK2 · rs11692570
See detailed info → SensitiveASTN2 · rs1372330
See detailed info → Sensitivenear CECR2 · rs5749032
See detailed info → SensitiveSCFD2 · rs17082301
See detailed info → SensitiveATOH8 · rs13402783
See detailed info → SensitiveBBS9 · rs3815652
See detailed info → Sensitivenear KIF16B · rs2327990
See detailed info → Sensitivenear SP9 · rs7582977
See detailed info →Showing 20 of 8459 · page 24 of 423
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.