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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NDRG1
(S152N +3 more)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease type 4D
GUncertain significance
NDRG1
(R148* +2 more)
Single nucleotide variant
(nonsense)
Charcot-Marie-Tooth disease type 4D
+2 more
GPathogenic
NDRG1
Single nucleotide variant
(splice acceptor variant)
Charcot-Marie-Tooth disease type 4D
GLikely pathogenic
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