rs3789875
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3789875(G;G) |
Make rs3789875(G;T) |
Make rs3789875(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 115033009 |
Gene | TNC |
is a | snp |
is | mentioned by |
dbSNP | rs3789875 |
dbSNP (classic) | rs3789875 |
ClinGen | rs3789875 |
ebi | rs3789875 |
HLI | rs3789875 |
Exac | rs3789875 |
Gnomad | rs3789875 |
Varsome | rs3789875 |
LitVar | rs3789875 |
Map | rs3789875 |
PheGenI | rs3789875 |
Biobank | rs3789875 |
1000 genomes | rs3789875 |
hgdp | rs3789875 |
ensembl | rs3789875 |
geneview | rs3789875 |
scholar | rs3789875 |
rs3789875 | |
pharmgkb | rs3789875 |
gwascentral | rs3789875 |
openSNP | rs3789875 |
23andMe | rs3789875 |
SNPshot | rs3789875 |
SNPdbe | rs3789875 |
MSV3d | rs3789875 |
GWAS Ctlg | rs3789875 |
GMAF | 0.1736 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 21298289] Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease