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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM2
(A618D +1 more)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease dominant intermediate B
+1 more
GPathogenic
DNM2
(P627R +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic