rs2131754

This is a regulatory region variant variant in the CRISPLD2 gene.

GWAS Catalog Trait Associations (1)

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

Inguinal hernia

Allele G
OR 1.09
p 3.0e-14
N 275,546
Major Consortium StudyLarge GWAS
European

About CRISPLD2

Predicted to enable glycosaminoglycan binding activity. Involved in face morphogenesis. Located in transport vesicle. [provided by Alliance of Genome Resources, Jul 2025]

View all CRISPLD2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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