rs2232367
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs2232367(C;T) |
Make rs2232367(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 49256855 |
Gene | FOXP3 |
is a | snp |
is | mentioned by |
dbSNP | rs2232367 |
dbSNP (classic) | rs2232367 |
ClinGen | rs2232367 |
ebi | rs2232367 |
HLI | rs2232367 |
Exac | rs2232367 |
Gnomad | rs2232367 |
Varsome | rs2232367 |
LitVar | rs2232367 |
Map | rs2232367 |
PheGenI | rs2232367 |
Biobank | rs2232367 |
1000 genomes | rs2232367 |
hgdp | rs2232367 |
ensembl | rs2232367 |
geneview | rs2232367 |
scholar | rs2232367 |
rs2232367 | |
pharmgkb | rs2232367 |
gwascentral | rs2232367 |
openSNP | rs2232367 |
23andMe | rs2232367 |
SNPshot | rs2232367 |
SNPdbe | rs2232367 |
MSV3d | rs2232367 |
GWAS Ctlg | rs2232367 |
GMAF | 0.02177 |
Max Magnitude | 0 |
[PMID 20412712] Defective FOXP3 expression in patients with acute Kawasaki disease and restoration by intravenous immunoglobulin therapy
[PMID 17526924] 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, |