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rs12347433

From SNPedia

Orientationplus
Stabilizedplus
Make rs12347433(C;C)
Make rs12347433(C;T)
Make rs12347433(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position115035318
GeneTNC
is asnp
is mentioned by
dbSNPrs12347433
ebirs12347433
HLIrs12347433
Exacrs12347433
Varsomers12347433
Maprs12347433
PheGenIrs12347433
hapmaprs12347433
1000 genomesrs12347433
hgdprs12347433
ensemblrs12347433
gopubmedrs12347433
geneviewrs12347433
scholarrs12347433
googlers12347433
pharmgkbrs12347433
gwascentralrs12347433
openSNPrs12347433
23andMers12347433
23andMe allrs12347433
SNP Nexus

SNPshotrs12347433
SNPdbers12347433
MSV3drs12347433
GWAS Ctlgrs12347433
GMAF0.1754
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21298289OA-icon.png] Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease