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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPV4
(W626* +4 more)
Single nucleotide variant
(nonsense)
Charcot-Marie-Tooth disease axonal type 2C
GLikely pathogenic
TRPV4
(R232H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
TRPV4
(S125Y +1 more)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease axonal type 2C
GUncertain significance
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