chrM:8361:G>A Detail (hg19) (MT-TK)

Information

Genome

Assembly Position
hg19 chrM:8,361-8,361
hg38 chrM:8,360-8,360 

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2003-12-01 no assertion criteria provided MERRF syndrome germline maternal Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
m.8361G>A AND MERRF syndrome ClinVar Detail
Gene
-
dbSNP
rs118192104 dbSNP
Genome
hg19
Position
chrM:8,361-8,361
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser