rs9263688
This is a upstream gene variant variant in the PSORS1C1 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
response to thioamide, Drug-induced agranulocytosis
Chen PL et al. “Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.” Nature Communications 6:7633 (2015)
Allele G
OR 8.06
p 5.0e-21
N 683
Small GWAS
East Asian
About PSORS1C1
This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]
View all PSORS1C1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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