chrM:10255:G>A Detail (hg19)

Information

Genome

Assembly Position
hg19 chrM:10,255-10,255
hg38 chrM:10,254-10,254 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

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
0.250 Leigh disease NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Gene
-
dbSNP
rs587776438 dbSNP
Genome
hg19
Position
chrM:10,255-10,255
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser