chrM:10254:G>A Detail (hg19) (MT-ND3)

Information

Genome

Assembly Position
hg19 chrM:10,254-10,254
hg38 chrM:10,253-10,253 

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance not provided
Review star
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
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NC_012920.1(MT-ND3):m.10254G>A AND Leigh syndrome ClinVar Detail
Gene
-
dbSNP
rs587776438 dbSNP
Genome
hg19
Position
chrM:10,254-10,254
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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