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rs4416533

From SNPedia

Orientationminus
Stabilizedminus
Make rs4416533(C;C)
Make rs4416533(C;T)
Make rs4416533(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position137405718
is asnp
is mentioned by
dbSNPrs4416533
ebirs4416533
HLIrs4416533
Exacrs4416533
Varsomers4416533
Maprs4416533
PheGenIrs4416533
hapmaprs4416533
1000 genomesrs4416533
hgdprs4416533
ensemblrs4416533
gopubmedrs4416533
geneviewrs4416533
scholarrs4416533
googlers4416533
pharmgkbrs4416533
gwascentralrs4416533
openSNPrs4416533
23andMers4416533
23andMe allrs4416533
SNP Nexus

SNPshotrs4416533
SNPdbers4416533
MSV3drs4416533
GWAS Ctlgrs4416533
GMAF0.4477
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4416533
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.59375
summary