rs12347433
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12347433(C;C) |
Make rs12347433(C;T) |
Make rs12347433(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 115035318 |
Gene | TNC |
is a | snp |
is | mentioned by |
dbSNP | rs12347433 |
dbSNP (classic) | rs12347433 |
ClinGen | rs12347433 |
ebi | rs12347433 |
HLI | rs12347433 |
Exac | rs12347433 |
Gnomad | rs12347433 |
Varsome | rs12347433 |
LitVar | rs12347433 |
Map | rs12347433 |
PheGenI | rs12347433 |
Biobank | rs12347433 |
1000 genomes | rs12347433 |
hgdp | rs12347433 |
ensembl | rs12347433 |
geneview | rs12347433 |
scholar | rs12347433 |
rs12347433 | |
pharmgkb | rs12347433 |
gwascentral | rs12347433 |
openSNP | rs12347433 |
23andMe | rs12347433 |
SNPshot | rs12347433 |
SNPdbe | rs12347433 |
MSV3d | rs12347433 |
GWAS Ctlg | rs12347433 |
GMAF | 0.1754 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21298289] Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease