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rs17806056

From SNPedia

Orientationplus
Stabilizedplus
Make rs17806056(A;A)
Make rs17806056(A;T)
Make rs17806056(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position11098642
GeneCLEC16A
is asnp
is mentioned by
dbSNPrs17806056
ebirs17806056
HLIrs17806056
Exacrs17806056
Varsomers17806056
Maprs17806056
PheGenIrs17806056
hapmaprs17806056
1000 genomesrs17806056
hgdprs17806056
ensemblrs17806056
gopubmedrs17806056
geneviewrs17806056
scholarrs17806056
googlers17806056
pharmgkbrs17806056
gwascentralrs17806056
openSNPrs17806056
23andMers17806056
23andMe allrs17806056
SNP Nexus

SNPshotrs17806056
SNPdbers17806056
MSV3drs17806056
GWAS Ctlgrs17806056
Max Magnitude
? (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]