212 positions on this site are linked to Schizophrenia, out of 113,826 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
MATN1 · rs12407717
See detailed info → SensitiveBMPR1B · rs17616243
See detailed info → SensitiveACADS · rs78885399
See detailed info → SensitiveSPHKAP · rs10204933
See detailed info → SensitiveSLC1A1 · rs1471786
See detailed info → SensitiveMEGF10 · rs72790443
See detailed info → SensitiveCNTN4 · rs17022006
See detailed info → SensitiveSLC1A1 · rs16921385
See detailed info → SensitiveCDSN · rs111782145
See detailed info → SensitiveLOC728586 · rs2764766
See detailed info → SensitiveSLC9B1 · rs11722779
See detailed info → SensitiveNDST3 · rs4833558
See detailed info → SensitiveMICC · rs115687605
See detailed info → SensitiveCHRNA3 · rs28681284
See detailed info → SensitiveCACNA1C · rs2239063
See detailed info → SensitiveHIST1H2APS2 · rs629444
See detailed info → SensitiveHLA-DQB1 · rs77296290
See detailed info → SensitiveTRIM26 · rs116408368
See detailed info → SensitiveSUMO2P1 · rs138488080
See detailed info → SensitiveTRNAS17 · rs115031589
See detailed info →Showing 20 of 212 · page 3 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.