chr16:89529580:>T Detail (hg38) (SPG7)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr16:89,595,988-89,595,988 |
| hg38 | chr16:89,529,580-89,529,580 |
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 |
|---|---|---|---|---|---|
| 0.560 | SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | NA | CLINVAR | Detail |
Annotation
Genome browser