214 positions on this site are linked to Schizophrenia, out of 114,120 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near LUZP2 · rs12360997
See detailed info → Sensitivenear NMB · rs12908161
See detailed info → Sensitivenear ASPG · rs112973353
See detailed info → Sensitivenear RPP21 · rs114200269
See detailed info → SensitiveCENPM · rs1023500
See detailed info → SensitivePEPD · rs10425465
See detailed info → Sensitivenear NMUR2 · rs79212538
See detailed info → SensitiveSDCCAG8 · rs77149735
See detailed info → SensitiveEPC2 · rs76355118
See detailed info → SensitiveNEU1 · rs67682613
See detailed info → SensitiveMCL1 · rs72700829
See detailed info → SensitiveCARMIL1 · rs62392365
See detailed info → SensitiveZNF804A · rs62200787
See detailed info → SensitiveH2BC11 · rs55834529
See detailed info → SensitivePPP1R16B · rs6065094
See detailed info → SensitiveMIR3679 · rs6430491
See detailed info → SensitiveRTN1 · rs2182139
See detailed info → SensitiveCNTN4 · rs11708578
See detailed info → SensitiveEGR1 · rs13164092
See detailed info → SensitiveAMBRA1 · rs61882743
See detailed info →Showing 20 of 214 · page 7 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.