rs1323555
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1323555(C;C) |
Make rs1323555(C;T) |
Make rs1323555(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 48676861 |
Gene | CYSLTR2 |
is a | snp |
is | mentioned by |
dbSNP | rs1323555 |
dbSNP (classic) | rs1323555 |
ClinGen | rs1323555 |
ebi | rs1323555 |
HLI | rs1323555 |
Exac | rs1323555 |
Gnomad | rs1323555 |
Varsome | rs1323555 |
LitVar | rs1323555 |
Map | rs1323555 |
PheGenI | rs1323555 |
Biobank | rs1323555 |
1000 genomes | rs1323555 |
hgdp | rs1323555 |
ensembl | rs1323555 |
geneview | rs1323555 |
scholar | rs1323555 |
rs1323555 | |
pharmgkb | rs1323555 |
gwascentral | rs1323555 |
openSNP | rs1323555 |
23andMe | rs1323555 |
SNPshot | rs1323555 |
SNPdbe | rs1323555 |
MSV3d | rs1323555 |
GWAS Ctlg | rs1323555 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24792382] |
Trait | Response to inhaled corticosteroid treatment in asthma (percentage change of FEV1) |
Title | Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid. |
Risk Allele | |
P-val | 2E-6 |
Odds Ratio | .34 [NR] unit increase |