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rs4522336

From SNPedia

Orientationplus
Stabilizedplus
Make rs4522336(C;C)
Make rs4522336(C;T)
Make rs4522336(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position48556315
is asnp
is mentioned by
dbSNPrs4522336
ebirs4522336
HLIrs4522336
Exacrs4522336
Varsomers4522336
Maprs4522336
PheGenIrs4522336
hapmaprs4522336
1000 genomesrs4522336
hgdprs4522336
ensemblrs4522336
gopubmedrs4522336
geneviewrs4522336
scholarrs4522336
googlers4522336
pharmgkbrs4522336
gwascentralrs4522336
openSNPrs4522336
23andMers4522336
23andMe allrs4522336
SNP Nexus

SNPshotrs4522336
SNPdbers4522336
MSV3drs4522336
GWAS Ctlgrs4522336
GMAF0.1042
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4522336
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.117188
summary