rs7746553

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

complement factor B measurement

Allele G
OR 0.30
p 4.0e-14
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

glycoprotein measurement

Allele G
OR 0.02
p 2.0e-8
N 199,732
Large GWAS
European

age at first sexual intercourse measurement

Allele C
OR 0.02
p 5.0e-8
N 397,338
Large GWAS
European

Research that mentions this SNP (1)

Polymorphisms in complement system genes and risk of non‐Hodgkin lymphoma
AssociationN=926Bryan A. Bassig et al.(2012)· Environmental and Molecular Mutagenesis

This case-control study of 432 cases and 494 controls examined polymorphisms in complement system genes and risk of non-Hodgkin lymphoma (NHL). A significant association was found with C1RL rs3813729 (C>T), which decreased NHL risk (OR=0.60, 95% CI=0.42-0.87, P=0.0062) and DLBCL risk (OR=0.39, 95% CI=0.20-0.73, P=0.0034). Additional associations were found with C1QG rs12756603 for CLL/SLL, and C2 rs497309 and C3 rs344550 for marginal zone lymphoma, though these were based on small case numbers.

Traits studied:Chronic lymphocytic leukemia/small lymphocytic lymphomaDiffuse large B-cell lymphomaFollicular lymphomaMarginal zone lymphomaNon-Hodgkin lymphoma

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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