rs7591163
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7591163(C;C) |
Make rs7591163(C;T) |
Make rs7591163(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 227850659 |
is a | snp |
is | mentioned by |
dbSNP | rs7591163 |
dbSNP (classic) | rs7591163 |
ClinGen | rs7591163 |
ebi | rs7591163 |
HLI | rs7591163 |
Exac | rs7591163 |
Gnomad | rs7591163 |
Varsome | rs7591163 |
LitVar | rs7591163 |
Map | rs7591163 |
PheGenI | rs7591163 |
Biobank | rs7591163 |
1000 genomes | rs7591163 |
hgdp | rs7591163 |
ensembl | rs7591163 |
geneview | rs7591163 |
scholar | rs7591163 |
rs7591163 | |
pharmgkb | rs7591163 |
gwascentral | rs7591163 |
openSNP | rs7591163 |
23andMe | rs7591163 |
SNPshot | rs7591163 |
SNPdbe | rs7591163 |
MSV3d | rs7591163 |
GWAS Ctlg | rs7591163 |
GMAF | 0.3554 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903302] |
Trait | Blood pressure |
Title | Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness |
Risk Allele | |
P-val | 2.9999999999999999E-7 |
Odds Ratio | NR NR |