rs17806056
This is a intron variant variant in the CLEC16A 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.
common variable immunodeficiency
Li J et al. “Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells.” Nature Communications 6:6804 (2015)
Allele A
OR 0.66
p 2.0e-9
N 11,777
Large GWAS
European
About CLEC16A
This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
View all CLEC16A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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