rs821577
This variant is located in the DISC1 gene.
▶Research that mentions this SNP (2)
▶DISC1 in adult ADHD patients: An association study in two European samplesAssociationN=2,703Kaya K. Jacobsen et al.(2013)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
This is the first systematic study examining the role of DISC1 gene variants in adult ADHD. The intronic SNP rs1538979 was associated with ADHD in a Norwegian sample (OR 1.33, p=0.03) and replicated in a Spanish sample using the tagging SNP rs11122330 (meta-analysis p=0.008, OR 1.25). Additionally, the non-synonymous variant rs6675281 (Phe607Leu) was associated with positive bipolar spectrum symptoms as measured by the Mood Disorder Questionnaire (OR 1.44, p=0.01) in the Norwegian sample, though this was not replicated.
▶Association of Variants in DISC1 With Psychosis-Related Traits in a Large Population CohortAssociationN=4,527Liisa Tomppo et al.(2009)· Archives of General Psychiatry
Association study of 41 SNPs in DISC1 with psychosis-related traits (social anhedonia, physical anhedonia, perceptual aberration, schizoidia) in 4,651 participants from a Finnish birth cohort. Carriers of the minor allele of rs821577 had significantly higher social anhedonia scores (P<.001, d=0.09), and rs821633 showed significant interaction effects with rs821577 and rs1538979 on anhedonia phenotypes (P<.001, d=0.07-0.14).
About DISC1
This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1;11)(q42.1;q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
View all DISC1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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