{{Rsnum
|rsid=4866
|Gene=NUDT1
|Chromosome=7
|position=2249951
|Orientation=plus
|GMAF=0.02663
|Gene_s=NUDT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 4.5 | 95.5
| HCB | 0.0 | 8.1 | 91.9
| JPT | 0.0 | 20.5 | 79.5
| YRI | 0.0 | 5.6 | 94.4
| ASW | 0.0 | 5.3 | 94.7
| CHB | 0.0 | 8.1 | 91.9
| CHD | 0.0 | 9.2 | 90.8
| GIH | 0.0 | 2.0 | 98.0
| LWK | 0.0 | 4.7 | 95.3
| MEX | 0.0 | 3.5 | 96.5
| MKK | 0.0 | 7.1 | 92.9
| TSI | 0.0 | 3.0 | 97.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22720119
|Title=Association of base excision repair gene polymorphisms with ESRD risk in a Chinese population
|OA=1
}}

{{GET Evidence
|gene=NUDT1
|aa_change=Val106Met
|aa_change_short=V106M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4866
|overall_frequency_n=116
|overall_frequency_d=10758
|overall_frequency=0.0107827
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=2
|n_web_uneval=10
}}

{{PMID Auto
|PMID=19443904
|Title=Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma.
|OA=1
}}

{{PMID Auto
|PMID=23396182
|Title=Combined analysis of polymorphism variants in hMTH1, hOGG1 and MUTYH genes on the risk of type 2 diabetes in the Chinese population.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}