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rs2232367

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2232367(C;T)
Make rs2232367(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position49256855
GeneFOXP3
is asnp
is mentioned by
dbSNPrs2232367
ClinGenrs2232367
ebirs2232367
HLIrs2232367
Exacrs2232367
Varsomers2232367
Maprs2232367
PheGenIrs2232367
hapmaprs2232367
1000 genomesrs2232367
hgdprs2232367
ensemblrs2232367
gopubmedrs2232367
geneviewrs2232367
scholarrs2232367
googlers2232367
pharmgkbrs2232367
gwascentralrs2232367
openSNPrs2232367
23andMers2232367
23andMe allrs2232367
SNP Nexus

SNPshotrs2232367
SNPdbers2232367
MSV3drs2232367
GWAS Ctlgrs2232367
GMAF0.02177
Max Magnitude0

[PMID 20412712] Defective FOXP3 expression in patients with acute Kawasaki disease and restoration by intravenous immunoglobulin therapy


[PMID 17526924OA-icon.png] SNPs in the FOXP3 gene region show no association with Juvenile Idiopathic Arthritis in a UK Caucasian population.


ClinVar
Risk rs2232367(T;T)
Alt rs2232367(T;T)
Reference Rs2232367(C;C)
Significance Other
Disease not specified
Variation info
Gene FOXP3
CLNDBN not specified
Reversed 1
HGVS NC_000023.10:g.49113312G>A
CLNSRC ClinVar
CLNACC RCV000117096.1,