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rs17147528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17147528(C;C)
Make rs17147528(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position121270010
is asnp
is mentioned by
dbSNPrs17147528
ebirs17147528
HLIrs17147528
Exacrs17147528
Varsomers17147528
Maprs17147528
PheGenIrs17147528
hapmaprs17147528
1000 genomesrs17147528
hgdprs17147528
ensemblrs17147528
gopubmedrs17147528
geneviewrs17147528
scholarrs17147528
googlers17147528
pharmgkbrs17147528
gwascentralrs17147528
openSNPrs17147528
23andMers17147528
23andMe allrs17147528
SNP Nexus

SNPshotrs17147528
SNPdbers17147528
MSV3drs17147528
GWAS Ctlgrs17147528
GMAF0.06198
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs17147528
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0952381
summary