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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PMP22
(H121R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADORA2B, ARHGAP44
+18 more
Copy number loss
Hereditary liability to pressure palsies
Gnot provided