rs9332730

This variant is located in the C2;CFB gene.

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GWAS Catalog Trait Associations (1)

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

tenascin-X measurement

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)

Allele C

OR 0.29

p 3.0e-113

N 47,745

Large GWAS

European

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ClinVar annotation

Likely Benign★★★☆

5 submitters2 publications

Macular degeneration; Complement component 2 deficiency; Atypical hemolytic-uremic syndrome; Age related macular degeneration 14; not provided; not specified

View on ClinVar →

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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