rs2383208
| Orientation | plus |
| Stabilized | plus |
| Make rs2383208(A;A) |
| Make rs2383208(A;G) |
| Make rs2383208(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22132077 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2383208 |
| dbSNP (classic) | rs2383208 |
| ClinGen | rs2383208 |
| ebi | rs2383208 |
| HLI | rs2383208 |
| Exac | rs2383208 |
| Gnomad | rs2383208 |
| Varsome | rs2383208 |
| LitVar | rs2383208 |
| Map | rs2383208 |
| PheGenI | rs2383208 |
| Biobank | rs2383208 |
| 1000 genomes | rs2383208 |
| hgdp | rs2383208 |
| ensembl | rs2383208 |
| geneview | rs2383208 |
| scholar | rs2383208 |
| rs2383208 | |
| pharmgkb | rs2383208 |
| gwascentral | rs2383208 |
| openSNP | rs2383208 |
| 23andMe | rs2383208 |
| SNPshot | rs2383208 |
| SNPdbe | rs2383208 |
| MSV3d | rs2383208 |
| GWAS Ctlg | rs2383208 |
| GMAF | 0.2268 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [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 |
| Risk Allele | A |
| P-val | 2E-29 |
| Odds Ratio | 1.34 [1.27-1.41] |
[PMID 22096510] Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a chinese population
[PMID 18224336] Haplotypic analysis of Wellcome Trust Case Control Consortium data.
[PMID 18426861] Association analysis of type 2 diabetes Loci in type 1 diabetes.
[PMID 18852197] Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
[PMID 19096518] 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.
[PMID 19463184] Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.
[PMID 19578366] Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
[PMID 20386740] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
[PMID 21270277] The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.
| GWAS snp | |
|---|---|
| PMID | [PMID 23209189]
|
| Trait | Type 2 diabetes |
| Title | Genome-wide association study for type 2 diabetes in indians identifies a new susceptibility locus at 2q21. |
| Risk Allele | T |
| P-val | 3E-6 |
| Odds Ratio | 1.23 [1.13-1.34] |
| GWAS snp | |
|---|---|
| PMID | [PMID 22961080]
|
| Trait | Type 2 diabetes |
| Title | A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. |
| Risk Allele | A |
| P-val | 3E-17 |
| Odds Ratio | 1.22 [1.17-1.28] |
[PMID 26499758] Association of type 2 diabetes GWAS loci and the risk of Parkinson's and Alzheimer's diseases
[PMID 29432124] CDKN2A/B T2D GWAS Risk-SNPs Impact Locus Gene Expression and Proliferation in Human Islets.
[PMID 31543200] Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.
