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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POMGNT2
(R158H)
Single nucleotide variant
(missense variant)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
+1 more
GConflicting classifications of pathogenicity
WDR81
(G282E)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GLikely pathogenic
MT-TV
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GPathogenic/Likely pathogenic
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