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rs4767551

From SNPedia

Orientationplus
Stabilizedplus
Make rs4767551(C;C)
Make rs4767551(C;T)
Make rs4767551(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position117516255
GeneKSR2
is asnp
is mentioned by
dbSNPrs4767551
ebirs4767551
HLIrs4767551
Exacrs4767551
Varsomers4767551
Maprs4767551
PheGenIrs4767551
hapmaprs4767551
1000 genomesrs4767551
hgdprs4767551
ensemblrs4767551
gopubmedrs4767551
geneviewrs4767551
scholarrs4767551
googlers4767551
pharmgkbrs4767551
gwascentralrs4767551
openSNPrs4767551
23andMers4767551
23andMe allrs4767551
SNP Nexus

SNPshotrs4767551
SNPdbers4767551
MSV3drs4767551
GWAS Ctlgrs4767551
GMAF0.4105
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4767551
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.40625
summary