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rs2288553

From SNPedia

Orientationplus
Stabilizedplus
Make rs2288553(A;A)
Make rs2288553(A;T)
Make rs2288553(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position128409647
GeneIMPDH1
is asnp
is mentioned by
dbSNPrs2288553
ebirs2288553
HLIrs2288553
Exacrs2288553
Varsomers2288553
Maprs2288553
PheGenIrs2288553
hapmaprs2288553
1000 genomesrs2288553
hgdprs2288553
ensemblrs2288553
gopubmedrs2288553
geneviewrs2288553
scholarrs2288553
googlers2288553
pharmgkbrs2288553
gwascentralrs2288553
openSNPrs2288553
23andMers2288553
23andMe allrs2288553
SNP Nexus

SNPshotrs2288553
SNPdbers2288553
MSV3drs2288553
GWAS Ctlgrs2288553
GMAF0.1212
Max Magnitude

[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.