rs9834970
This is a intergenic variant variant.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
bipolar I disorder
bipolar disorder
▶Research that mentions this SNP (2)
▶Genetic analysis of SNPs in CACNA1C and ANK3 gene with schizophrenia: A comprehensive meta‐analysisAssociationN=1,237Fayi Nie et al.(2015)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
A case-control association study of 1,237 Pakistani subjects (479 with major depression, 222 with bipolar disorder, 146 with schizophrenia, 390 controls) examined 11 dopaminergic system gene variants. Significant risk associations were found for rs1006737 and rs2238056 (CACNA1c) with bipolar disorder (OR=1.14-1.15), while rs10033951 (DRD5), rs2388334 (POU3F2), and the DRD4 120bp VNTR showed protective effects across disorders (OR=0.81-0.86).
▶Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorderAssociationN=411Rodrigo Secolin et al.(2013)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Family-based association study in 74 families (96 bipolar affective disorder patients) identified rs166508 in intron 15 of the ITGA9 gene as significantly associated with bipolar disorder (P=0.0187). The rs166508 A allele showed upregulation of ITGA9 transcripts (Kruskal-Wallis P=0.0339) and was associated with an intronic deletion (r.1689_1839del) affecting exon 16, which contains microRNA binding sites that may regulate ITGA9 expression.
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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