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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIEZO2
(R2686H +1 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, distal, with impaired proprioception and touch
+6 more
GPathogenic
PIEZO2
Deletion
(intron variant)
Arthrogryposis, distal, with impaired proprioception and touch
+5 more
GBenign
PIEZO2
(V1219M +1 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, distal, with impaired proprioception and touch
+1 more
GConflicting classifications of pathogenicity
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