rs1320267
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1320267(C;C) |
Make rs1320267(C;G) |
Make rs1320267(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 126012137 |
is a | snp |
is | mentioned by |
dbSNP | rs1320267 |
dbSNP (classic) | rs1320267 |
ClinGen | rs1320267 |
ebi | rs1320267 |
HLI | rs1320267 |
Exac | rs1320267 |
Gnomad | rs1320267 |
Varsome | rs1320267 |
LitVar | rs1320267 |
Map | rs1320267 |
PheGenI | rs1320267 |
Biobank | rs1320267 |
1000 genomes | rs1320267 |
hgdp | rs1320267 |
ensembl | rs1320267 |
geneview | rs1320267 |
scholar | rs1320267 |
rs1320267 | |
pharmgkb | rs1320267 |
gwascentral | rs1320267 |
openSNP | rs1320267 |
23andMe | rs1320267 |
SNPshot | rs1320267 |
SNPdbe | rs1320267 |
MSV3d | rs1320267 |
GWAS Ctlg | rs1320267 |
GMAF | 0.4183 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903303![]() |
Trait | Other subclinical atherosclerosis traits |
Title | Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study |
Risk Allele | |
P-val | 0.0000069999999999999999 |
Odds Ratio | NR NR |