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rs4562389

From SNPedia

Orientationplus
Stabilizedplus
Make rs4562389(C;C)
Make rs4562389(C;T)
Make rs4562389(T;T)
ReferenceGRCh37 37.1/131
Chromosome9
Position8805462
GenePTPRD
is asnp
is mentioned by
dbSNPrs4562389
ebirs4562389
HLIrs4562389
Exacrs4562389
Varsomers4562389
Maprs4562389
PheGenIrs4562389
hapmaprs4562389
1000 genomesrs4562389
hgdprs4562389
ensemblrs4562389
gopubmedrs4562389
geneviewrs4562389
scholarrs4562389
googlers4562389
pharmgkbrs4562389
gwascentralrs4562389
openSNPrs4562389
23andMers4562389
23andMe allrs4562389
SNP Nexus

SNPshotrs4562389
SNPdbers4562389
MSV3drs4562389
GWAS Ctlgrs4562389
GMAF0.3421
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs4562389
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.620968
summary