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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MME
(L110*)
Single nucleotide variant
(nonsense)
Charcot-Marie-Tooth disease axonal type 2T
GLikely pathogenic
MME
(K525T)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease axonal type 2T
GUncertain significance