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rs11171806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11171806(A;A)
Make rs11171806(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position56339747
GeneIL23A
is asnp
is mentioned by
dbSNPrs11171806
dbSNP (classic)rs11171806
ClinGenrs11171806
ebirs11171806
HLIrs11171806
Exacrs11171806
Gnomadrs11171806
Varsomers11171806
LitVarrs11171806
Maprs11171806
PheGenIrs11171806
Biobankrs11171806
1000 genomesrs11171806
hgdprs11171806
ensemblrs11171806
geneviewrs11171806
scholarrs11171806
googlers11171806
pharmgkbrs11171806
gwascentralrs11171806
openSNPrs11171806
23andMers11171806
SNPshotrs11171806
SNPdbers11171806
MSV3drs11171806
GWAS Ctlgrs11171806
GMAF0.04408
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23579029] Protective effect of interleukin-23A (IL23A) haplotype variants on type 1A diabetes mellitus in a Brazilian population


[PMID 23673284] Association study in Romanians confirms IL23A gene haplotype block rs2066808/rs11171806 as conferring risk to psoriatic arthritis


[PMID 17236132OA-icon.png] A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.


[PMID 20154336OA-icon.png] Comprehensive sequence analysis of the human IL23A gene defines new variation content and high rate of evolutionary conservation.


[PMID 25670394] Both interleukin-23A polymorphism and serum interlukin-23 expression are associated with Graves' disease risk


ClinVar
Risk rs11171806(A;A)
Alt rs11171806(A;A)
Reference Rs11171806(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene IL23A
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.56733531G>A
CLNSRC
CLNACC RCV000455797.1,



[PMID 27320770] Impact of the IL-17F, IL-23 and IL-23R on susceptibility and phenotype of systemic lupus erythematosus.