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rs11706052

From SNPedia

Orientationplus
Stabilizedplus
Make rs11706052(A;A)
Make rs11706052(A;G)
Make rs11706052(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position49026677
GeneIMPDH2
is asnp
is mentioned by
dbSNPrs11706052
ebirs11706052
HLIrs11706052
Exacrs11706052
Varsomers11706052
Maprs11706052
PheGenIrs11706052
hapmaprs11706052
1000 genomesrs11706052
hgdprs11706052
ensemblrs11706052
gopubmedrs11706052
geneviewrs11706052
scholarrs11706052
googlers11706052
pharmgkbrs11706052
gwascentralrs11706052
openSNPrs11706052
23andMers11706052
23andMe allrs11706052
SNP Nexus

SNPshotrs11706052
SNPdbers11706052
MSV3drs11706052
GWAS Ctlgrs11706052
GMAF0.07254
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19770842] An inosine 5'-monophosphate dehydrogenase 2 single-nucleotide polymorphism impairs the effect of mycophenolic acid



[PMID 20679962OA-icon.png] Polymorphisms in type I and II inosine monophosphate dehydrogenase genes and association with clinical outcome in patients on mycophenolate mofetil


[PMID 21996196] Lymphocyte Counts in Kidney Allograft Recipients Are Associated With IMPDH2 3757T>C Gene Polymorphism


[PMID 21955043OA-icon.png] Validation of single nucleotide polymorphisms associated with acute rejection in kidney transplant recipients using a large multi-center cohort


[PMID 19617864] Interpatient variability in IMPDH activity in MMF-treated renal transplant patients is correlated with IMPDH type II 3757T > C polymorphism.


[PMID 20061166] Genetic polymorphisms influence mycophenolate mofetil-related adverse events in pediatric heart transplant patients.


GET Evidence
rs11706052
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0777096
summary



[PMID 22960765] Inosine monophosphate dehydrogenase polymorphisms and renal allograft outcome.