rs1106908

This variant is located in the GGNBP2 gene.

GWAS Catalog Trait Associations (1)

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

body mass index

Allele A
OR 0.02
p 8.0e-23
N 806,834
Meta-analysisLarge GWAS
European
Allele A
OR 0.03
p 5.0e-20
N 153,950
Large GWAS
East Asian

ClinVar annotation

Benign
1 submitter

GGNBP2-related disorder

View on ClinVar →

About GGNBP2

Predicted to be involved in spermatogenesis. Predicted to act upstream of or within several processes, including labyrinthine layer blood vessel development; negative regulation of cell population proliferation; and negative regulation of peptidyl-tyrosine phosphorylation. Predicted to be located in cytoplasmic vesicle. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2025]

View all GGNBP2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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