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rs4459653

From SNPedia

Orientationplus
Stabilizedplus
Make rs4459653(C;C)
Make rs4459653(C;T)
Make rs4459653(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44095462
GeneZNF224
is asnp
is mentioned by
dbSNPrs4459653
ebirs4459653
HLIrs4459653
Exacrs4459653
Varsomers4459653
Maprs4459653
PheGenIrs4459653
hapmaprs4459653
1000 genomesrs4459653
hgdprs4459653
ensemblrs4459653
gopubmedrs4459653
geneviewrs4459653
scholarrs4459653
googlers4459653
pharmgkbrs4459653
gwascentralrs4459653
openSNPrs4459653
23andMers4459653
23andMe allrs4459653
SNP Nexus

SNPshotrs4459653
SNPdbers4459653
MSV3drs4459653
GWAS Ctlgrs4459653
GMAF0.2902
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4459653
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.777778
summary