rs11160190
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11160190(A;A) |
Make rs11160190(A;G) |
Make rs11160190(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 94546047 |
is a | snp |
is | mentioned by |
dbSNP | rs11160190 |
dbSNP (classic) | rs11160190 |
ClinGen | rs11160190 |
ebi | rs11160190 |
HLI | rs11160190 |
Exac | rs11160190 |
Gnomad | rs11160190 |
Varsome | rs11160190 |
LitVar | rs11160190 |
Map | rs11160190 |
PheGenI | rs11160190 |
Biobank | rs11160190 |
1000 genomes | rs11160190 |
hgdp | rs11160190 |
ensembl | rs11160190 |
geneview | rs11160190 |
scholar | rs11160190 |
rs11160190 | |
pharmgkb | rs11160190 |
gwascentral | rs11160190 |
openSNP | rs11160190 |
23andMe | rs11160190 |
SNPshot | rs11160190 |
SNPdbe | rs11160190 |
MSV3d | rs11160190 |
GWAS Ctlg | rs11160190 |
GMAF | 0.3329 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22907691] |
Trait | Vaspin levels |
Title | Genetic variation in the vaspin gene affects circulating serum vaspin concentrations. |
Risk Allele | G |
P-val | 4E-41 |
Odds Ratio | .04 [NR] unit decrease |