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rs2873892

From SNPedia

Orientationplus
Stabilizedplus
Make rs2873892(A;A)
Make rs2873892(A;G)
Make rs2873892(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position139234730
is asnp
is mentioned by
dbSNPrs2873892
ebirs2873892
HLIrs2873892
Exacrs2873892
Varsomers2873892
Maprs2873892
PheGenIrs2873892
hapmaprs2873892
1000 genomesrs2873892
hgdprs2873892
ensemblrs2873892
gopubmedrs2873892
geneviewrs2873892
scholarrs2873892
googlers2873892
pharmgkbrs2873892
gwascentralrs2873892
openSNPrs2873892
23andMers2873892
23andMe allrs2873892
SNP Nexus

SNPshotrs2873892
SNPdbers2873892
MSV3drs2873892
GWAS Ctlgrs2873892
Merged fromRs4552883
GMAF0.2401
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.