rs116446171
This is a regulatory region variant variant.
▶GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Waldenstrom macroglobulinemia
McMaster ML et al. “Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia.” Nature Communications 9(1):4182 (2018)
Allele G
OR 21.14
p 1.0e-54
N 4,015
Large GWAS
European
immunoglobulin J chain 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 0.20
p 2.0e-23
N 47,745
Large GWAS
European
diffuse large B-cell lymphoma
Cerhan JR et al. “Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.” Nature Genetics 46(11):1233-8 (2014)
Allele G
OR 2.20
p 2.0e-21
N 11,523
Large GWAS
European
CD5 antigen-like 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 0.16
p 1.0e-17
N 47,745
Large GWAS
European
plasma protein metabolism disease
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.42
p 2.0e-15
N 627,057
Major Consortium StudyLarge GWAS
multi-ancestry
eosinophil percentage of leukocytes
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 5.0e-14
N 394,642
Large GWAS
European
central nervous system non-hodgkin lymphoma
Labreche K et al. “A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network study.” Neuro-oncology 21(8):1039-1048 (2019)
Allele G
OR 4.99
p 2.0e-13
N 1,609
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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