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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM2
(R290Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
DNM2
(R465W)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic