Rs72558186

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is asnp
is mentioned by
dbSNPrs72558186
hapmaprs72558186
hgdprs72558186
ensemblrs72558186
gopubmedrs72558186
scholarrs72558186
googlers72558186
pharmgkbrs72558186
hgvbaseg2prs72558186
medrefsnprs72558186
23andMers72558186
SNP Nexus

Chromosome10
Orientationplus
Position96531745
GenotypeEffect
rs72558186(A;A)CYP2C19*7 homozygote
rs72558186(A;T)carrier of one CYP2C19*7 allele
rs72558186(T;T)normal


Genotypes Magnitude Summary
Rs72558186(A;A) CYP2C19*7 homozygote
Rs72558186(A;T) carrier of one CYP2C19*7 allele
Rs72558186(T;T) normal
The rs72558186(A) SNP represents a CYP2C19 allele known as CYP2C19*7; it reflects a splice donor mutation that leads to a poor metabolizer phenotype.[PMID 10411572]

This SNP is also known as CYP2C19_19294T>A, and in the Affymetrix DMET panel, as DMET3B10072.

Note: absence of allele frequency data leaves this as a possible ambiguous flip.