rs2288553
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2288553(A;A) |
| Make rs2288553(A;T) |
| Make rs2288553(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 128409647 |
| Gene | IMPDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2288553 |
| dbSNP (classic) | rs2288553 |
| ClinGen | rs2288553 |
| ebi | rs2288553 |
| HLI | rs2288553 |
| Exac | rs2288553 |
| Gnomad | rs2288553 |
| Varsome | rs2288553 |
| LitVar | rs2288553 |
| Map | rs2288553 |
| PheGenI | rs2288553 |
| Biobank | rs2288553 |
| 1000 genomes | rs2288553 |
| hgdp | rs2288553 |
| ensembl | rs2288553 |
| geneview | rs2288553 |
| scholar | rs2288553 |
| rs2288553 | |
| pharmgkb | rs2288553 |
| gwascentral | rs2288553 |
| openSNP | rs2288553 |
| 23andMe | rs2288553 |
| SNPshot | rs2288553 |
| SNPdbe | rs2288553 |
| MSV3d | rs2288553 |
| GWAS Ctlg | rs2288553 |
| GMAF | 0.1212 |
| Max Magnitude | 0 |
[PMID 20649757
] Inosine 5'-monophosphate dehydrogenase 1 haplotypes and association with mycophenolate mofetil gastrointestinal intolerance in pediatric heart transplant patients
[PMID 16384941] 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.
