{{Rsnum
|rsid=1801262
|Gene=NEUROD1
|Chromosome=2
|position=181678728
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.2658
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NEUROD1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.8 | 46.0 | 37.2
| HCB | 0.0 | 18.2 | 81.8
| JPT | 0.9 | 13.3 | 85.8
| YRI | 5.4 | 38.1 | 56.5
| ASW | 3.5 | 43.9 | 52.6
| CHB | 0.0 | 18.2 | 81.8
| CHD | 0.9 | 18.7 | 80.4
| GIH | 6.0 | 34.0 | 60.0
| LWK | 4.5 | 38.2 | 57.3
| MEX | 10.3 | 36.2 | 53.4
| MKK | 11.5 | 45.5 | 42.9
| TSI | 20.6 | 42.2 | 37.3
| HapMapRevision=28
}}{{Report GE
|PubMed=17192490
|Source=pubmed
|AffyProbeset=SNP_A-2314121
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=1
|rsid=1801262
|ancestral=G
|RiskPopulation=NEU(Finnland)
|RiskAllele=A
|CaseFreq=0.37
|ControlFreq=0.34
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.15
|Disease=Type II Diabetes
|DiseaseSymbol=T2D
}}

rs1801262 increases susceptibility to Type II Diabetes 1.15 times for carriers of the A allele {{PMID|17192490}}
{{Venter SNP
|rsid=1801262
|allele=C
|frequency=0.6
|uid=1103658307448
|type=homozygous_SNP
|hugo=NEUROD1
|ensembl gene=ENSG00000162992
|ensembl transcript=ENST00000295108
|sift=TOLERATED
|disease=Defects in NEUROD1 are a cause of maturity onset diabetes of the young type VI (MODY6) (MIM:606394). MODY6 is characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion.
}}

{{PMID|14681825|OA=1
}} Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).

{{PMID|16909454|OA=1
}} NeuroD1 gene and interleukin-18 gene polymorphisms in type 1 diabetes in Dalmatian population of Southern Croatia.

{{PMID|20416077|OA=1
}} Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

{{GET Evidence
|gene=NEUROD1
|aa_change=Thr45Ala
|aa_change_short=T45A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1801262
|overall_frequency_n=7231
|overall_frequency_d=10758
|overall_frequency=0.672151
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=82
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=1
|autoscore=2
|n_web_uneval=3
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}