rs11126936
This variant is located in the SLC30A3 gene.
▶Research that mentions this SNP (1)
▶Neural effects of the CSMD1 genome‐wide associated schizophrenia risk variant rs10503253ReviewEmma J. Rose et al.(2013)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
A comprehensive review of the genetics and epigenetics of schizophrenia, covering candidate gene associations, genome-wide association studies (GWAS), gene expression studies, and epigenetic mechanisms. The review highlights major GWAS findings including associations with CSMD1 (rs10503253), CACNA1C (rs4765905), SLC30A3 (rs11126936, rs11126929), VRK2 (rs2312147), MPC2 (rs10489202), miR-137 (rs1625579), and MKL1 (rs6001946), while discussing the complex polygenic architecture of the disorder with heritability estimated at 81-85%.
About SLC30A3
Enables zinc ion transmembrane transporter activity. Involved in zinc ion import into lysosome. Located in late endosome and synaptic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
View all SLC30A3 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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