|Dataset||GWASdb SNP-Disease Associations|
|Category||disease or phenotype associations|
|Description||A B cell deficiency that is an autosomal recessive disorder caused by mutation in the IgA (CD79 alpha) antigen receptor. (Human Disease Ontology, DOID_0060025)|
|Downloads & Tools|
1 genes associated with the disease immunoglobulin alpha deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
|TNFSF13||tumor necrosis factor (ligand) superfamily, member 13||1.26953|