rs2131755

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

GWAS Catalog Trait Associations (3)

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

Inguinal hernia

Allele G
OR 1.09
p 2.0e-14
N 275,546
Major Consortium StudyLarge GWAS
European

diverticular disease

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.05
p 3.0e-13
N 560,597
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR
β 0.003
p 2.0e-10
N 409,728
Large GWAS
European

glomerular filtration rate

Allele G
OR 6.59
p 4.0e-11
N 1,508,659
Large GWAS
multi-ancestry

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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