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rs2278294

From SNPedia

Orientationminus
Stabilizedminus
Make rs2278294(A;A)
Make rs2278294(A;G)
Make rs2278294(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position128400645
GeneIMPDH1
is asnp
is mentioned by
dbSNPrs2278294
ebirs2278294
HLIrs2278294
Exacrs2278294
Varsomers2278294
Maprs2278294
PheGenIrs2278294
hapmaprs2278294
1000 genomesrs2278294
hgdprs2278294
ensemblrs2278294
gopubmedrs2278294
geneviewrs2278294
scholarrs2278294
googlers2278294
pharmgkbrs2278294
gwascentralrs2278294
openSNPrs2278294
23andMers2278294
23andMe allrs2278294
SNP Nexus

SNPshotrs2278294
SNPdbers2278294
MSV3drs2278294
GWAS Ctlgrs2278294
GMAF0.3999
Max Magnitude
? (A;A) (A;G) (G;G) 28
[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 20649757OA-icon.png] Inosine 5'-monophosphate dehydrogenase 1 haplotypes and association with mycophenolate mofetil gastrointestinal intolerance in pediatric heart transplant patients


[PMID 16384941OA-icon.png] Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.


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


[PMID 20136638] Correlation of IMPDH1 gene polymorphisms with subclinical acute rejection and mycophenolic acid exposure parameters on day 28 after renal transplantation.


GET Evidence
rs2278294
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.398438
summary



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