Have questions? Visit https://www.reddit.com/r/SNPedia

rs3789875

From SNPedia

Orientationminus
Stabilizedminus
Make rs3789875(G;G)
Make rs3789875(G;T)
Make rs3789875(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position115033009
GeneTNC
is asnp
is mentioned by
dbSNPrs3789875
dbSNP (old)rs3789875
ClinGenrs3789875
ebirs3789875
HLIrs3789875
Exacrs3789875
Gnomadrs3789875
Varsomers3789875
Maprs3789875
PheGenIrs3789875
Biobankrs3789875
1000 genomesrs3789875
hgdprs3789875
ensemblrs3789875
gopubmedrs3789875
geneviewrs3789875
scholarrs3789875
googlers3789875
pharmgkbrs3789875
gwascentralrs3789875
openSNPrs3789875
23andMers3789875
23andMe allrs3789875
SNP Nexus

SNPshotrs3789875
SNPdbers3789875
MSV3drs3789875
GWAS Ctlgrs3789875
GMAF0.1736
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 21298289OA-icon.png] Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease