{{Rsnum
|rsid=4974081
|Gene=QRICH1
|Chromosome=3
|position=49033066
|Orientation=plus
|GMAF=0.1249
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=QRICH1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 35.4 | 56.6
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 16.3 | 82.3
| ASW | 1.8 | 14.0 | 84.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 4.0 | 96.0
| LWK | 1.8 | 27.3 | 70.9
| MEX | 0.0 | 20.7 | 79.3
| MKK | 1.9 | 30.8 | 67.3
| TSI | 4.9 | 33.3 | 61.8
| HapMapRevision=28
}}{{PMID|18976158}} An in silico functional analysis using FASTSNP predicts that this rs4974081 (-3624 A/G) could be a potential transcription factor binding site. This finding suggests that rs4974081 could be a good candidate SNP for association studies with immunosuppressive and chemotherapeutic therapy outcomes.

{{PMID Auto
|PMID=20679962
|Title=Polymorphisms in type I and II inosine monophosphate dehydrogenase genes and association with clinical outcome in patients on mycophenolate mofetil
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}