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rs924080

From SNPedia

Orientationplus
Stabilizedplus
Make rs924080(C;C)
Make rs924080(C;T)
Make rs924080(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67294457
is asnp
is mentioned by
dbSNPrs924080
dbSNP (classic)rs924080
ClinGenrs924080
ebirs924080
HLIrs924080
Exacrs924080
Gnomadrs924080
Varsomers924080
LitVarrs924080
Maprs924080
PheGenIrs924080
Biobankrs924080
1000 genomesrs924080
hgdprs924080
ensemblrs924080
geneviewrs924080
scholarrs924080
googlers924080
pharmgkbrs924080
gwascentralrs924080
openSNPrs924080
23andMers924080
SNPshotrs924080
SNPdbers924080
MSV3drs924080
GWAS Ctlgrs924080
GMAF0.3972
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20622878OA-icon.png]
Trait Behcet's disease
Title Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease
Risk Allele
P-val 7E-9
Odds Ratio 1.28 [1.18-1.39]


[PMID 17068223OA-icon.png] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.


[PMID 22076442OA-icon.png] A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations.


[PMID 22378604] Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behcet's disease.


[PMID 24151497OA-icon.png] Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet's Disease Risk in Western Algeria


[PMID 31814470] Association of Interleukin-23R Gene Polymorphisms with Behcet's Disease Susceptibility: A Meta-Analysis of Case-control Studies.