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rs4148947

From SNPedia

Orientationplus
Stabilizedplus
Make rs4148947(C;C)
Make rs4148947(C;T)
Make rs4148947(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position72010359
GeneCHST3
is asnp
is mentioned by
dbSNPrs4148947
ClinGenrs4148947
ebirs4148947
HLIrs4148947
Exacrs4148947
Varsomers4148947
Maprs4148947
PheGenIrs4148947
hapmaprs4148947
1000 genomesrs4148947
hgdprs4148947
ensemblrs4148947
gopubmedrs4148947
geneviewrs4148947
scholarrs4148947
googlers4148947
pharmgkbrs4148947
gwascentralrs4148947
openSNPrs4148947
23andMers4148947
23andMe allrs4148947
SNP Nexus

SNPshotrs4148947
SNPdbers4148947
MSV3drs4148947
GWAS Ctlgrs4148947
GMAF0.3177
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4148947
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.328125
summary