chr22:19968739:>C Detail (hg38) (COMT)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr22:19,956,262-19,956,262 |
| hg38 | chr22:19,968,739-19,968,739 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| 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 |
|---|---|---|---|---|---|
| 0.329 | attention deficit hyperactivity disorder | Gene-gene interaction analysis revealed significant additive effect of DBH rs110... | BeFree | 21216270 | Detail |
| 0.178 | attention deficit hyperactivity disorder | Gene-gene interaction analysis revealed significant additive effect of DBH rs110... | BeFree | 21216270 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Gene-gene interaction analysis revealed significant additive effect of DBH rs1108580 and DRD4 rs1800... | DisGeNET | Detail |
| Gene-gene interaction analysis revealed significant additive effect of DBH rs1108580 and DRD4 rs1800... | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs362204 dbSNP
- Genome
- hg38
- Position
- chr22:19,968,739-19,968,739
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- C
Genome browser