chr6:132570322:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr6:132,891,461-132,892,498 |
| hg38 | chr6:132,570,322-132,571,359 |
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 |
|---|---|---|---|---|---|
| <0.001 | Mental Depression | NA | BeFree | Detail | |
| <0.001 | depressive disorder | NA | BeFree | Detail | |
| 0.140 | schizophrenia | NA | BeFree,CTD_human,GAD,LHGDN | Detail | |
| <0.001 | Unipolar Depression | NA | BeFree | Detail | |
| <0.001 | Mental Depression | In this study we investigated for the first time the possible association betwee... | BeFree | 20493543 | Detail |
| <0.001 | major depressive disorder | NA | BeFree | Detail | |
| 0.006 | bipolar disorder | We have further studied a previously investigated sample of 187 major depressive... | BeFree | 19582769 | Detail |
| 0.006 | bipolar disorder | NA | BeFree,GAD,LHGDN | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| In this study we investigated for the first time the possible association between a set of TAAR6 gen... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| We have further studied a previously investigated sample of 187 major depressive disorder (MDD) pati... | DisGeNET | Detail |
| NA | 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
- rs7452939 dbSNP
- Genome
- hg38
- Position
- chr6:132,570,322-132,571,359
- Variant Type
- snv
Genome browser