rs7844723
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7844723(C;C) |
Make rs7844723(C;T) |
Make rs7844723(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 121896264 |
is a | snp |
is | mentioned by |
dbSNP | rs7844723 |
dbSNP (classic) | rs7844723 |
ClinGen | rs7844723 |
ebi | rs7844723 |
HLI | rs7844723 |
Exac | rs7844723 |
Gnomad | rs7844723 |
Varsome | rs7844723 |
LitVar | rs7844723 |
Map | rs7844723 |
PheGenI | rs7844723 |
Biobank | rs7844723 |
1000 genomes | rs7844723 |
hgdp | rs7844723 |
ensembl | rs7844723 |
geneview | rs7844723 |
scholar | rs7844723 |
rs7844723 | |
pharmgkb | rs7844723 |
gwascentral | rs7844723 |
openSNP | rs7844723 |
23andMe | rs7844723 |
SNPshot | rs7844723 |
SNPdbe | rs7844723 |
MSV3d | rs7844723 |
GWAS Ctlg | rs7844723 |
GMAF | 0.2925 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903294] |
Trait | Hemostatic factors and hematological phenotypes |
Title | Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study |
Risk Allele | |
P-val | 0.0000019999999999999999 |
Odds Ratio | NR NR |