212 positions on this site are linked to Schizophrenia, out of 113,994 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
IMMP2L · rs13240464
See detailed info → SensitiveMIR548AJ2 · rs215411
See detailed info → SensitiveCCDC39 · rs9841616
See detailed info → SensitiveCACNB2 · rs7893279
See detailed info → SensitiveDRD2 · rs2514218
See detailed info → SensitiveIGSF9B · rs75059851
See detailed info → SensitiveMLL5 · rs6466055
See detailed info → SensitiveFUT9 · rs117074560
See detailed info → SensitiveMAN2A1 · rs4388249
See detailed info → SensitiveGRM3 · rs12704290
See detailed info → SensitiveCACNA1C · rs2007044
See detailed info → SensitiveKDM4A · rs11210892
See detailed info → SensitiveLRRIQ3 · rs12129573
See detailed info → SensitiveFANCL · rs11682175
See detailed info → SensitiveANP32E · rs140505938
See detailed info → SensitiveIMMP2L · rs211829
See detailed info → SensitiveCHADL · rs9607782
See detailed info → SensitiveHHAT · rs7527939
See detailed info → SensitiveNDST3 · rs11098403
See detailed info → SensitiveGIGYF2 · rs778371
See detailed info →Showing 20 of 212 · page 10 of 11
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.