rs77956314

GWAS Catalog Trait Associations (11)

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

hippocampal volume

Allele C
OR 123.31
p 2.0e-35
N 21,297
Large GWAS
European
Hibar DP et al. Novel genetic loci associated with hippocampal volume. Nature Communications 8:13624 (2017)
Allele C
OR 10.42
p 2.0e-25
N 26,814
Large GWAS
multi-ancestry
Klein M et al. Genetic Markers of ADHD-Related Variations in Intracranial Volume. The American Journal of Psychiatry 176(3):228-238 (2019)
Allele C
OR 9.53
p 2.0e-21
N 24,704
Large GWAS
European

hippocampal CA1 volume

Allele C
OR 24.08
p 7.0e-28
N 21,297
Large GWAS
European

granule cell layer dentate gyrus volume

Allele C
OR 11.01
p 9.0e-26
N 21,297
Large GWAS
European

hippocampus molecular layer volume

Allele C
OR 19.27
p 2.0e-25
N 21,297
Large GWAS
European

hippocampal CA4 volume

Allele C
OR 9.26
p 2.0e-24
N 21,297
Large GWAS
European

hippocampal formation volume

Allele C
OR 20.52
p 2.0e-19
N 21,297
Large GWAS
European

subiculum volume

Allele C
OR 12.96
p 1.0e-17
N 21,297
Large GWAS
European

hippocampal CA3 volume

Allele C
OR 7.79
p 2.0e-15
N 21,297
Large GWAS
European

brain volume, hippocampal volume

Allele T
OR 55.18
p 3.0e-15
N 13,171
Large GWAS
multi-ancestry

hippocampal amigdala transition area volume

Allele C
OR 2.04
p 4.0e-13
N 21,297
Large GWAS
European

Research that mentions this SNP (1)

The Role of Clusterin, Complement Receptor 1, and Phosphatidylinositol Binding Clathrin Assembly Protein in Alzheimer Disease Risk and Cerebrospinal Fluid Biomarker Levels
MethodsN=30,717Brit-Maren M. Schjeide et al.(2011)· Archives of General Psychiatry

This paper presents a novel bioinformatics method combining Gene Ontology (GO) with stratified false discovery rate (sFDR) analysis to prioritize genes for imaging genetics studies. Applied to ENIGMA2 GWAS meta-analysis data of hippocampal volume (N=30,717 individuals, 6,570,616 SNPs), the transport system gene network identified SNPs with sFDR q-values between 10-20%, including rs117831534 and rs118025365 in TESC (p=4.91e-07 and 4e-07), and multiple SNPs in SLC4A10 and KCNH7. The method demonstrates improved statistical power for discovering imaging genetic biomarkers without excessive multiple testing burden.

Traits studied:Alzheimer's diseaseHippocampal volume

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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