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rs11188072

From SNPedia

Orientationplus
Stabilizedplus
Make rs11188072(C;C)
Make rs11188072(C;T)
Make rs11188072(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position94759304
is asnp
is mentioned by
dbSNPrs11188072
ebirs11188072
HLIrs11188072
Exacrs11188072
Varsomers11188072
Maprs11188072
PheGenIrs11188072
hapmaprs11188072
1000 genomesrs11188072
hgdprs11188072
ensemblrs11188072
gopubmedrs11188072
geneviewrs11188072
scholarrs11188072
googlers11188072
pharmgkbrs11188072
gwascentralrs11188072
openSNPrs11188072
23andMers11188072
23andMe allrs11188072
SNP Nexus

SNPshotrs11188072
SNPdbers11188072
MSV3drs11188072
GWAS Ctlgrs11188072
GMAF0.1534
Max Magnitude



GET Evidence
rs11188072
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.195312
summary



[PMID 23661171] CYP2C19 genotypes and their impact on clopidogrel responsiveness in percutaneous coronary intervention