rs3809272

GWAS Catalog Trait Associations (5)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

platelet count

Allele A
OR 0.09
p 4.0e-126
N 166,066
Large GWAS
European

mitochondrial DNA measurement

Allele A
OR 0.02
p 7.0e-17
N 295,150
Large GWAS
European

testosterone measurement

Allele A
OR 0.02
p 4.0e-13
N 235,096
Large GWAS
European
Allele A
OR 0.02
p 4.0e-10
N 194,453
Large GWAS
European

immature platelet measurement

Allele A
OR 0.05
p 4.0e-10
N 36,829
Large GWAS
European

cup-to-disc ratio measurement

Allele G
OR 0.03
p 1.0e-8
N 89,579
Large GWAS
European

Research that mentions this SNP (1)

Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356
AssociationN=721Beate Glaser et al.(2005)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

This LD mapping study identified significant associations between bipolar affective disorder and genetic markers on chromosome 12q23-q24. Two SNPs (rs3847953, P=0.002 and rs933399, P=0.004) and an insertion/deletion (rs3840795, P=0.005) in regions containing CUX2 and FLJ32356 genes showed significant association after Bonferroni correction in 347 bipolar cases and 374 controls.

Traits studied:Bipolar I disorderBipolar affective disorder

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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