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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PMP22
(Y130*)
Single nucleotide variant
(nonsense +1 more)
not provided
GLikely pathogenic
PMP22
(T118M)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
PMP22
(S72L)
Single nucleotide variant
(missense variant +1 more)
Charcot-Marie-Tooth disease, type IA
+3 more
GPathogenic
PMP22
(H51R)
Single nucleotide variant
(missense variant +1 more)
Charcot-Marie-Tooth disease, type I
+2 more
GConflicting classifications of pathogenicity
PMP22
(D37H)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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