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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126860531, NDRG1
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease type 4
+6 more
GConflicting classifications of pathogenicity
LOC126860531, NDRG1
(V177A +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126860531, NDRG1
Single nucleotide variant
(intron variant)
Charcot-Marie-Tooth disease type 4D
+3 more
GBenign
LOC126860531, NDRG1
Single nucleotide variant
(intron variant)
Charcot-Marie-Tooth disease
+3 more
GBenign
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