chr9:22010413:A>G Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr9:22,010,412-22,010,412 View the variant detail on this assembly version. |
| hg38 | chr9:22,010,413-22,010,413 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.322 | Diabetes Mellitus, Non-Insulin-Dependent | The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... | BeFree | 20384434 | Detail |
| 0.452 | Diabetes Mellitus, Non-Insulin-Dependent | The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... | BeFree | 20384434 | Detail |
| 0.010 | Impaired glucose tolerance | The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... | BeFree | 20384434 | Detail |
| <0.001 | Impaired glucose tolerance | The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... | BeFree | 20384434 | Detail |
| 0.083 | Diabetes Mellitus, Non-Insulin-Dependent | [Our results suggest that combining genetic markers with traditional clinical ri... | GAD | 20384434 | Detail |
| 0.002 | Glucose Metabolism Disorders | [Our results suggest that combining genetic markers with traditional clinical ri... | GAD | 20384434 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six variants (IGF2BP2 rs44029... | DisGeNET | Detail |
| The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six variants (IGF2BP2 rs44029... | DisGeNET | Detail |
| The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six variants (IGF2BP2 rs44029... | DisGeNET | Detail |
| The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six variants (IGF2BP2 rs44029... | DisGeNET | Detail |
| [Our results suggest that combining genetic markers with traditional clinical risk factors has the p... | DisGeNET | Detail |
| [Our results suggest that combining genetic markers with traditional clinical risk factors has the p... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs495490 dbSNP
- Genome
- hg38
- Position
- chr9:22,010,413-22,010,413
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
Genome browser