{{Rsnum
|rsid=2383208
|Chromosome=9
|position=22132077
|Orientation=plus
|GMAF=0.2268
|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 | 63.7 | 31.0 | 5.3
| HCB | 38.1 | 41.8 | 20.1
| JPT | 27.7 | 53.6 | 18.8
| YRI | 76.9 | 20.4 | 2.7
| ASW | 63.2 | 29.8 | 7.0
| CHB | 38.1 | 41.8 | 20.1
| CHD | 30.3 | 51.4 | 18.3
| GIH | 82.0 | 18.0 | 0.0
| LWK | 62.7 | 30.9 | 6.4
| MEX | 77.6 | 20.7 | 1.7
| MKK | 50.0 | 37.2 | 12.8
| TSI | 67.6 | 27.5 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19401414
|Trait=Type 2 diabetes
|Title=Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
|RiskAllele=A
|Pval=2E-29
|OR=1.34
|ORtxt=[1.27-1.41]
|OA=1
}}

{{PMID Auto
|PMID=22096510
|Title=Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a chinese population
|OA=1
}}

{{PMID Auto
|PMID=18224336
|Title=Haplotypic analysis of Wellcome Trust Case Control Consortium data.
|OA=1
}}

{{PMID Auto
|PMID=18426861
|Title=Association analysis of type 2 diabetes Loci in type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=18852197
|Title=Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
|OA=1
}}

{{PMID Auto
|PMID=19096518
|Title=Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=19463184
|Title=Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.
|OA=1
}}

{{PMID Auto
|PMID=19578366
|Title=Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
|OA=1
}}

{{PMID Auto
|PMID=20386740
|Title=Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
|OA=1
}}

{{PMID Auto
|PMID=21270277
|Title=The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2383208
|overall_frequency_n=23
|overall_frequency_d=128
|overall_frequency=0.179688
|n_genomes=14
|n_genomes_annotated=0
|n_haplomes=18
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23209189
  |Trait=Type 2 diabetes
  |Title=Genome-wide association study for type 2 diabetes in indians identifies a new susceptibility locus at 2q21.
  |RiskAllele=T
  |Pval=3E-6
  |OR=1.23
  |ORtxt=[1.13-1.34]
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=22961080
  |Trait=Type 2 diabetes
  |Title=A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.
  |RiskAllele=A
  |Pval=3E-17
  |OR=1.22
  |ORtxt=[1.17-1.28]
  |OA=1
}}

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