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rs2146807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2146807(C;C)
Make rs2146807(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position44318290
is asnp
is mentioned by
dbSNPrs2146807
ebirs2146807
HLIrs2146807
Exacrs2146807
Varsomers2146807
Maprs2146807
PheGenIrs2146807
hapmaprs2146807
1000 genomesrs2146807
hgdprs2146807
ensemblrs2146807
gopubmedrs2146807
geneviewrs2146807
scholarrs2146807
googlers2146807
pharmgkbrs2146807
gwascentralrs2146807
openSNPrs2146807
23andMers2146807
23andMe allrs2146807
SNP Nexus

SNPshotrs2146807
SNPdbers2146807
MSV3drs2146807
GWAS Ctlgrs2146807
GMAF0.1575
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 18979498OA-icon.png] rs2146807 association with the fatality of acute coronary event