rs3766680
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3766680(A;A) |
Make rs3766680(A;G) |
Make rs3766680(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 175327312 |
Gene | LOC105371623, TNR |
is a | snp |
is | mentioned by |
dbSNP | rs3766680 |
dbSNP (classic) | rs3766680 |
ClinGen | rs3766680 |
ebi | rs3766680 |
HLI | rs3766680 |
Exac | rs3766680 |
Gnomad | rs3766680 |
Varsome | rs3766680 |
LitVar | rs3766680 |
Map | rs3766680 |
PheGenI | rs3766680 |
Biobank | rs3766680 |
1000 genomes | rs3766680 |
hgdp | rs3766680 |
ensembl | rs3766680 |
geneview | rs3766680 |
scholar | rs3766680 |
rs3766680 | |
pharmgkb | rs3766680 |
gwascentral | rs3766680 |
openSNP | rs3766680 |
23andMe | rs3766680 |
SNPshot | rs3766680 |
SNPdbe | rs3766680 |
MSV3d | rs3766680 |
GWAS Ctlg | rs3766680 |
GMAF | 0.4578 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.0000039999999999999998 |
Odds Ratio | NR NR |