rs56036302
This is a intron variant variant in the TSBP1 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Sjogren syndrome
Sakaue S et al. “A cross-population atlas of genetic associations for 220 human phenotypes.” Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.67
p 6.0e-10
N 175,902
Large GWAS
East Asian
Autoimmune Hepatitis
Sakaue S et al. “A cross-population atlas of genetic associations for 220 human phenotypes.” Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 1.24
p 7.0e-9
N 166,614
Large GWAS
East Asian
About TSBP1
Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
View all TSBP1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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