chrM:10254:G>A Detail (hg38) (MT-ND3)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chrM:10,255-10,255 View the variant detail on this assembly version. |
| hg38 | chrM:10,254-10,254 |
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
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
not provided
|
no assertion provided | Leigh syndrome |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.250 | Leigh disease | NA | CLINVAR | Detail |
Annotation
Genome browser