rs17226566
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17226566(C;C) |
Make rs17226566(C;T) |
Make rs17226566(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 74007677 |
Gene | LY96 |
is a | snp |
is | mentioned by |
dbSNP | rs17226566 |
dbSNP (classic) | rs17226566 |
ClinGen | rs17226566 |
ebi | rs17226566 |
HLI | rs17226566 |
Exac | rs17226566 |
Gnomad | rs17226566 |
Varsome | rs17226566 |
LitVar | rs17226566 |
Map | rs17226566 |
PheGenI | rs17226566 |
Biobank | rs17226566 |
1000 genomes | rs17226566 |
hgdp | rs17226566 |
ensembl | rs17226566 |
geneview | rs17226566 |
scholar | rs17226566 |
rs17226566 | |
pharmgkb | rs17226566 |
gwascentral | rs17226566 |
openSNP | rs17226566 |
23andMe | rs17226566 |
SNPshot | rs17226566 |
SNPdbe | rs17226566 |
MSV3d | rs17226566 |
GWAS Ctlg | rs17226566 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24902762] Genetic variants in endotoxin signalling pathway, domestic endotoxin exposure and asthma exacerbations