rs6065926
▶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.
low affinity immunoglobulin epsilon Fc receptor measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele G
OR 0.08
p 1.0e-41
N 47,745
Large GWAS
European
B-cell receptor CD22 level
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele G
OR 0.06
p 6.0e-28
N 47,745
Large GWAS
European
level of T-cell leukemia/lymphoma protein 1A 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 G
OR 0.05
p 1.0e-16
N 47,745
Large GWAS
European
Graves disease
White SL et al. “Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases.” Nature Genetics 58(2):307-316 (2026)
Allele G
OR 0.10
p 9.0e-11
N 1,881,665
Large GWAS
European
CD40 measurement
Caron B et al. “Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes.” Genome Medicine 14(1):28 (2022)
Allele G
OR 0.15
p 1.0e-10
N 400
Small GWAS
European
multiple sclerosis
Sorosina M et al. “A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility.” Journal of Neurology 269(8):4510-4522 (2022)
Allele A
OR 1.16
p 9.0e-9
N 4,046
Large GWAS
European
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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