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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ9
(L108R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
COQ9
(V150A)
Single nucleotide variant
(missense variant)
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
GUncertain significance