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rs17879685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP2C19*13 allele
(T;T) CYP2C19*13 homozygote
ReferenceGRCh38 38.1/142
Chromosome10
Position94849995
GeneCYP2C19
is asnp
is mentioned by
dbSNPrs17879685
ebirs17879685
HLIrs17879685
Exacrs17879685
Varsomers17879685
Maprs17879685
PheGenIrs17879685
hapmaprs17879685
1000 genomesrs17879685
hgdprs17879685
ensemblrs17879685
gopubmedrs17879685
geneviewrs17879685
scholarrs17879685
googlers17879685
pharmgkbrs17879685
gwascentralrs17879685
openSNPrs17879685
23andMers17879685
23andMe allrs17879685
SNP Nexus

SNPshotrs17879685
SNPdbers17879685
MSV3drs17879685
GWAS Ctlgrs17879685
GMAF0.005051
Max Magnitude0
? (C;C) (C;T) (T;T) 28

The rs17879685(T) SNP defines the CYP2C19 allele known as CYP2C19*13.


GET Evidence
CYP2C19-R410C
aa_change Arg410Cys
aa_change_short R410C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.015625
summary