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rs4552883

From SNPedia

Merged intors2873892
Orientationplus
Stabilizedplus
Make rs4552883(A;A)
Make rs4552883(A;G)
Make rs4552883(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position139234730
is asnp
is mentioned by
dbSNPrs4552883
ebirs4552883
HLIrs4552883
Exacrs4552883
Varsomers4552883
Maprs4552883
PheGenIrs4552883
hapmaprs4552883
1000 genomesrs4552883
hgdprs4552883
ensemblrs4552883
gopubmedrs4552883
geneviewrs4552883
scholarrs4552883
googlers4552883
pharmgkbrs4552883
gwascentralrs4552883
openSNPrs4552883
23andMers4552883
23andMe allrs4552883
SNP Nexus

SNPshotrs4552883
SNPdbers4552883
MSV3drs4552883
GWAS Ctlgrs4552883
StatusMerged into rs2873892
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21298289OA-icon.png] Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease