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.
BCL11B · rs10150710
See detailed info → SensitiveTMTC1 · rs439639
See detailed info → SensitiveSLC22A8 · rs4149181
See detailed info → Sensitivenear LINC01645 · rs17659437
See detailed info → Sensitivenear KCNIP1 · rs76131026
See detailed info → SensitiveRGS6 · rs7143919
See detailed info → Sensitivenear WDR11 · rs117043183
See detailed info → SensitiveHLA-DQA1 · rs115443066
See detailed info → SensitivePTPRD · rs3824417
See detailed info → SensitiveDPYD · rs61789073
See detailed info → SensitiveLINC01470 · rs10515678
See detailed info → SensitiveCTC-436P18.1 · rs72761442
See detailed info → SensitiveZSWIM6 · rs6449528
See detailed info → Sensitivenear LINC02730 · rs4936216
See detailed info → SensitiveMIR100HG · rs117752187
See detailed info → SensitiveHLA-DRB1 · rs147976543
See detailed info → SensitiveCFAP77 · rs187751347
See detailed info → SensitiveHLA-DRB1 · rs11753207
See detailed info → Sensitivenear HLA-DRB5 · rs116182620
See detailed info → SensitiveLINC02997 · rs572938512
See detailed info →Showing 20 of 212 · page 1 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.