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rs7102569

From SNPedia

Orientationplus
Stabilizedplus
Make rs7102569(A;A)
Make rs7102569(A;G)
Make rs7102569(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position79473855
is asnp
is mentioned by
dbSNPrs7102569
ebirs7102569
HLIrs7102569
Exacrs7102569
Varsomers7102569
Maprs7102569
PheGenIrs7102569
hapmaprs7102569
1000 genomesrs7102569
hgdprs7102569
ensemblrs7102569
gopubmedrs7102569
geneviewrs7102569
scholarrs7102569
googlers7102569
pharmgkbrs7102569
gwascentralrs7102569
openSNPrs7102569
23andMers7102569
23andMe allrs7102569
SNP Nexus

SNPshotrs7102569
SNPdbers7102569
MSV3drs7102569
GWAS Ctlgrs7102569
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24816038] In search for genetic determinants of clinically meaningful differential cardiovascular event reduction by pravastatin in the PHArmacogenetic study of Statins in the Elderly at risk (PHASE)/PROSPER study