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Links from MedGen

Items: 3

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrMT:10197
GRCh38:
ChrMT:10197
MT-ND3Mitochondrial diseasePathogenic
(Jul 25, 2022)
reviewed by expert panel
FDA Recognized Database
2.
GRCh37:
ChrMT:10158
GRCh38:
ChrMT:10158
MT-ND3Mitochondrial diseasePathogenic
(Oct 26, 2021)
reviewed by expert panel
FDA Recognized Database
3.
GRCh37:
ChrMT:10191
GRCh38:
ChrMT:10191
MT-ND3Mitochondrial diseasePathogenic
(Aug 23, 2022)
reviewed by expert panel
FDA Recognized Database
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