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rs4436578

From SNPedia

Orientationplus
Stabilizedplus
Make rs4436578(C;C)
Make rs4436578(C;T)
Make rs4436578(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position113436043
GeneDRD2
is asnp
is mentioned by
dbSNPrs4436578
ebirs4436578
HLIrs4436578
Exacrs4436578
Varsomers4436578
Maprs4436578
PheGenIrs4436578
hapmaprs4436578
1000 genomesrs4436578
hgdprs4436578
ensemblrs4436578
gopubmedrs4436578
geneviewrs4436578
scholarrs4436578
googlers4436578
pharmgkbrs4436578
gwascentralrs4436578
openSNPrs4436578
23andMers4436578
23andMe allrs4436578
SNP Nexus

SNPshotrs4436578
SNPdbers4436578
MSV3drs4436578
GWAS Ctlgrs4436578
GMAF0.3489
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4436578
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.66129
summary