rs17806056
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17806056(A;A) |
Make rs17806056(A;T) |
Make rs17806056(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 11098642 |
Gene | CLEC16A |
is a | snp |
is | mentioned by |
dbSNP | rs17806056 |
dbSNP (classic) | rs17806056 |
ClinGen | rs17806056 |
ebi | rs17806056 |
HLI | rs17806056 |
Exac | rs17806056 |
Gnomad | rs17806056 |
Varsome | rs17806056 |
LitVar | rs17806056 |
Map | rs17806056 |
PheGenI | rs17806056 |
Biobank | rs17806056 |
1000 genomes | rs17806056 |
hgdp | rs17806056 |
ensembl | rs17806056 |
geneview | rs17806056 |
scholar | rs17806056 |
rs17806056 | |
pharmgkb | rs17806056 |
gwascentral | rs17806056 |
openSNP | rs17806056 |
23andMe | rs17806056 |
SNPshot | rs17806056 |
SNPdbe | rs17806056 |
MSV3d | rs17806056 |
GWAS Ctlg | rs17806056 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
778 Common variable immunodeficiency disorder (CVID) cases compared with 10,999 controls using the Illumina Immunochip; the first non-HLA genome-wide significant risk for CVID locus was found within the CLEC16A gene, namely rs17806056. The minor allele, rs17806056(A), is associated with reduced risk for CVID (odds ratio 0.66, CI: 0.57 - 0.75, p=2.0 × 10e-9).[PMID 25891430]