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Items: 1 to 100 of 103

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
not provided
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Duplication
Oxyphilic adenoma
GPathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Mediastinal germ cell tumor
+1 more
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
+1 more
GBenign/Likely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
not provided
GLikely benign
MT-ND6
Single nucleotide variant
not provided
GBenign
MT-ND6
Single nucleotide variant
Cognitive impairment
+6 more
GUncertain significance
MT-ND6
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Mitochondrial disease
GPathogenic
MT-ND6
Single nucleotide variant
Mitochondrial disease
GPathogenic
MT-ND6
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leber optic atrophy
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Deletion
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Mitochondrial cytopathy
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leber optic atrophy and dystonia
GPathogenic
MT-ND6
Single nucleotide variant
Dysarthria
+3 more
GConflicting classifications of pathogenicity
MT-ND6
Single nucleotide variant
Leigh syndrome
+2 more
GConflicting classifications of pathogenicity
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ND6
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND6
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND6
Single nucleotide variant
Mitochondrial DNA-related disorder
Gnot provided
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