rs1518395
This is a intron variant variant in the VRK2 gene.
▶GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
schizophrenia
major depressive disorder
wellbeing measurement
▶Research that mentions this SNP (1)
▶Evaluation of the relationship between VRK2, rs4380187 polymorphisms, and genetic susceptibility to schizophrenia in the Chinese Han populationAssociationN=986Xianglai Liu et al.(2021)· The Journal of Gene Medicine
A case-control study in 493 Chinese Han schizophrenia patients and 493 controls found that the C allele of rs4380187 (near ZNF804A) was significantly associated with decreased schizophrenia risk (OR=0.79, 95% CI: 0.66-0.94, p=0.008). The AA genotype showed significantly lower frequency in cases (OR=0.62, p=0.009), and associations were stronger in males (OR=0.64-0.68, p=0.002-0.003) and individuals aged ≥36 years.
About VRK2
This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. The encoded protein acts as an effector of signaling pathways that regulate apoptosis and tumor cell growth. Variants in this gene have been associated with schizophrenia. Alternative splicing results in multiple transcript variants that differ in their subcellular localization and biological activity. [provided by RefSeq, Jan 2014]
View all VRK2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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