rs142428017
This variant is located in the BCL9 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.
level of lysophosphatidic acid phosphatase type 6 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 0.54
p 4.0e-12
N 47,745
Large GWAS
European
▶ClinVar annotation
Conflicting Classifications
5 submitters2 publicationsnot provided; BCL9-related disorder; not specified
View on ClinVar →About BCL9
BCL9 is associated with B-cell acute lymphoblastic leukemia. It may be a target of translocation in B-cell malignancies with abnormalities of 1q21. Its function is unknown. The overexpression of BCL9 may be of pathogenic significance in B-cell malignancies. [provided by RefSeq, Jul 2008]
View all BCL9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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