chrM:10198:G>A Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chrM:10,198-10,198 |
| hg38 | chrM:10,197-10,197 View the variant detail on this assembly version. |
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 |
|---|---|---|---|---|---|
| 0.120 | Leigh syndrome due to mitochondrial complex I deficiency | NA | CLINVAR | Detail | |
| 0.250 | Leigh disease | NA | CLINVAR | Detail | |
| 0.120 | Leber optic atrophy and dystonia | NA | CLINVAR | Detail |
Annotation
Genome browser