rs7009110
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7009110(C;C) |
Make rs7009110(C;T) |
Make rs7009110(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 80379644 |
is a | snp |
is | mentioned by |
dbSNP | rs7009110 |
dbSNP (classic) | rs7009110 |
ClinGen | rs7009110 |
ebi | rs7009110 |
HLI | rs7009110 |
Exac | rs7009110 |
Gnomad | rs7009110 |
Varsome | rs7009110 |
LitVar | rs7009110 |
Map | rs7009110 |
PheGenI | rs7009110 |
Biobank | rs7009110 |
1000 genomes | rs7009110 |
hgdp | rs7009110 |
ensembl | rs7009110 |
geneview | rs7009110 |
scholar | rs7009110 |
rs7009110 | |
pharmgkb | rs7009110 |
gwascentral | rs7009110 |
openSNP | rs7009110 |
23andMe | rs7009110 |
SNPshot | rs7009110 |
SNPdbe | rs7009110 |
MSV3d | rs7009110 |
GWAS Ctlg | rs7009110 |
GMAF | 0.4858 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24388013] Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype