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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADH1C
(G78*)
Single nucleotide variant
(nonsense +1 more)
Parkinson disease, mitochondrial
Grisk factor
MT-TK
Single nucleotide variant
Mitochondrial disease
GPathogenic
MT-TP
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GBenign
MT-TT
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GUncertain significance
NDUFV2
(V29A)
Single nucleotide variant
(missense variant)
Mitochondrial complex 1 deficiency, nuclear type 7
+3 more
GBenign
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