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.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Inguinal hernia
Wei J et al. “Identification of fifty-seven novel loci for abdominal wall hernia development and their biological and clinical implications: results from the UK Biobank.” Hernia : the Journal of Hernias and Abdominal Wall Surgery 26(1):335-348 (2022)
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
Maguire LH et al. “Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease.” Nature Genetics 50(10):1359-1365 (2018)
Allele A
OR —
β 0.003
p 2.0e-10
N 409,728
Large GWAS
European
glomerular filtration rate
Liu H et al. “Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease.” Nature Genetics 54(7):950-962 (2022)
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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