Rs11188072

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is asnp
is mentioned by
dbSNPrs11188072
hapmaprs11188072
hgdprs11188072
ensemblrs11188072
gopubmedrs11188072
scholarrs11188072
googlers11188072
pharmgkbrs11188072
hgvbaseg2prs11188072
medrefsnprs11188072
23andMers11188072
SNP Nexus

Chromosome10
Orientationplus
Position96509050
GenotypeEffect
rs11188072(C;C)*?
rs11188072(C;T)*?
rs11188072(T;T)*?


PharmGKBPA161615688
NameCYP2C19: -3402C>T
AnnotationThis promoter variant is part of CYP2C19*17 haplotype, which causes increased acitivity and increased transcription of CYP2C19. Patients carrying this allele may exhibit a lack of response to commonly prescribed dosages of certain proton pump inhibitors (PPIs) and antidepressants, due to ultrarapid clearance of these drugs. CYP2C19*17 carriers are more likely to benifit from tamoxifen treatment.
GeneCYP2C19
Featue
EvidencePubMed ID:16413245; PubMed ID:17625515; PubMed ID:18294333
Drugsamitriptyline, citalopram, clomipramine, escitalopram, omeprazole, proguanil, tamoxifen
Diseases
Curation LevelCurated