215 positions on this site are linked to Schizophrenia, out of 114,204 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CA8 · rs867743
See detailed info → SensitiveAMBRA1 · rs61882743
See detailed info → SensitiveVRK2 · rs7596038
See detailed info → SensitiveHLA-DRB1 · rs41293330
See detailed info → SensitiveEGR1 · rs13164092
See detailed info → SensitiveRBKS · rs12623170
See detailed info → SensitiveCNTN4 · rs11708578
See detailed info → SensitiveTSNARE1 · rs4976976
See detailed info → SensitiveBTNL2 · rs116047537
See detailed info → SensitiveSAMD13 · rs2143757
See detailed info → SensitivePLCL1 · rs1837495
See detailed info → SensitiveHLA-B · rs116509918
See detailed info → SensitiveLOC10041978 · rs7807720
See detailed info → SensitiveHYAL3 · rs2073499
See detailed info → SensitiveLOC440704 · rs12139672
See detailed info → SensitiveGULOP · rs11778040
See detailed info → SensitiveMIR3679 · rs6430491
See detailed info → SensitiveFAM5B · rs6670165
See detailed info → SensitiveLETM2 · rs112537273
See detailed info → SensitiveVPS14C · rs12903146
See detailed info →Showing 20 of 215 · page 8 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.