S I D E B A R
Format
Sort by

Download:

Choose Destination

Links from PubMed

Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrMT:13708
GRCh38:
ChrMT:13708
MT-ND5Leber's optic atrophyConflicting interpretations of pathogenicity
(Sep 19, 2013)
no assertion criteria provided
2.
GRCh37:
ChrMT:14484
GRCh38:
ChrMT:14484
MT-ND6Leber's optic atrophy, Leigh syndromePathogenic
(Apr 17, 2014)
no assertion criteria provided