Have questions? Visit https://www.reddit.com/r/SNPedia

rs4148943

From SNPedia

Orientationplus
Stabilizedplus
Make rs4148943(C;C)
Make rs4148943(C;T)
Make rs4148943(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position72009749
GeneCHST3
is asnp
is mentioned by
dbSNPrs4148943
ebirs4148943
HLIrs4148943
Exacrs4148943
Varsomers4148943
Maprs4148943
PheGenIrs4148943
hapmaprs4148943
1000 genomesrs4148943
hgdprs4148943
ensemblrs4148943
gopubmedrs4148943
geneviewrs4148943
scholarrs4148943
googlers4148943
pharmgkbrs4148943
gwascentralrs4148943
openSNPrs4148943
23andMers4148943
23andMe allrs4148943
SNP Nexus

SNPshotrs4148943
SNPdbers4148943
MSV3drs4148943
GWAS Ctlgrs4148943
GMAF0.3586
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4148943
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.367188
summary