rs143612171

This is a intron variant variant in the HS6ST3 gene.

GWAS Catalog Trait Associations (1)

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

insomnia

Allele C
OR 0.03
p 1.0e-8
N 2,365,010
Meta-analysisLarge GWAS
European

About HS6ST3

Heparan sulfate (HS) sulfotransferases, such as HS6ST3, modify HS to generate structures required for interactions between HS and a variety of proteins. These interactions are implicated in proliferation and differentiation, adhesion, migration, inflammation, blood coagulation, and other diverse processes (Habuchi et al., 2000 [PubMed 10644753]).[supplied by OMIM, Mar 2008]

View all HS6ST3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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