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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD17B10
(R116Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
HSD17B10
(T108I)
Single nucleotide variant
(missense variant)
HSD10 mitochondrial disease
+2 more
GUncertain significance