rs188110518
This is a regulatory region variant variant in the STKLD1 gene.
▶GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
E-selectin amount
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.21
p 3.0e-24
N 47,745
Large GWAS
European
level of receptor-type tyrosine-protein phosphatase mu in blood
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.43
p 4.0e-24
N 47,745
Large GWAS
European
intercellular adhesion molecule 2 measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.20
p 1.0e-18
N 47,745
Large GWAS
European
podocalyxin measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.33
p 4.0e-14
N 47,745
Large GWAS
European
amount of neural cell adhesion molecule L1 (human) in blood
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.27
p 4.0e-12
N 47,745
Large GWAS
European
level of cadherin-17 in blood serum
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.26
p 5.0e-12
N 47,745
Large GWAS
European
About STKLD1
Predicted to enable protein serine/threonine kinase activity. [provided by Alliance of Genome Resources, Jul 2025]
View all STKLD1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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