rs4460176
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4460176(G;G) |
Make rs4460176(G;T) |
Make rs4460176(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 110161259 |
is a | snp |
is | mentioned by |
dbSNP | rs4460176 |
dbSNP (classic) | rs4460176 |
ClinGen | rs4460176 |
ebi | rs4460176 |
HLI | rs4460176 |
Exac | rs4460176 |
Gnomad | rs4460176 |
Varsome | rs4460176 |
LitVar | rs4460176 |
Map | rs4460176 |
PheGenI | rs4460176 |
Biobank | rs4460176 |
1000 genomes | rs4460176 |
hgdp | rs4460176 |
ensembl | rs4460176 |
geneview | rs4460176 |
scholar | rs4460176 |
rs4460176 | |
pharmgkb | rs4460176 |
gwascentral | rs4460176 |
openSNP | rs4460176 |
23andMe | rs4460176 |
SNPshot | rs4460176 |
SNPdbe | rs4460176 |
MSV3d | rs4460176 |
GWAS Ctlg | rs4460176 |
GMAF | 0.4954 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs4460176 |
PubMedID | [PMID 17903294] |
Condition | Hemostatic factors and hematological phenotypes |
Gene | Intergenic |
Risk Allele | |
pValue | 3.00E-006 |
OR | NA |
95% CI |
[PMID 17903299] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.