rs1367248
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1367248(G;G) |
Make rs1367248(G;T) |
Make rs1367248(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 124240787 |
Gene | CNTNAP5 |
is a | snp |
is | mentioned by |
dbSNP | rs1367248 |
dbSNP (classic) | rs1367248 |
ClinGen | rs1367248 |
ebi | rs1367248 |
HLI | rs1367248 |
Exac | rs1367248 |
Gnomad | rs1367248 |
Varsome | rs1367248 |
LitVar | rs1367248 |
Map | rs1367248 |
PheGenI | rs1367248 |
Biobank | rs1367248 |
1000 genomes | rs1367248 |
hgdp | rs1367248 |
ensembl | rs1367248 |
geneview | rs1367248 |
scholar | rs1367248 |
rs1367248 | |
pharmgkb | rs1367248 |
gwascentral | rs1367248 |
openSNP | rs1367248 |
23andMe | rs1367248 |
SNPshot | rs1367248 |
SNPdbe | rs1367248 |
MSV3d | rs1367248 |
GWAS Ctlg | rs1367248 |
GMAF | 0.1961 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903302![]() |
Trait | Tonometry |
Title | Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness |
Risk Allele | |
P-val | 0.0000030000000000000001 |
Odds Ratio | NR NR |