rs11204971
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11204971(A;A) |
Make rs11204971(A;G) |
Make rs11204971(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 152286602 |
is a | snp |
is | mentioned by |
dbSNP | rs11204971 |
dbSNP (classic) | rs11204971 |
ClinGen | rs11204971 |
ebi | rs11204971 |
HLI | rs11204971 |
Exac | rs11204971 |
Gnomad | rs11204971 |
Varsome | rs11204971 |
LitVar | rs11204971 |
Map | rs11204971 |
PheGenI | rs11204971 |
Biobank | rs11204971 |
1000 genomes | rs11204971 |
hgdp | rs11204971 |
ensembl | rs11204971 |
geneview | rs11204971 |
scholar | rs11204971 |
rs11204971 | |
pharmgkb | rs11204971 |
gwascentral | rs11204971 |
openSNP | rs11204971 |
23andMe | rs11204971 |
SNPshot | rs11204971 |
SNPdbe | rs11204971 |
MSV3d | rs11204971 |
GWAS Ctlg | rs11204971 |
GMAF | 0.2599 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22448455] Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis