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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIEZO2
(R2686H +1 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GPathogenic
PIEZO2
(R2686C +1 more)
Single nucleotide variant
(missense variant)
Gordon syndrome
+1 more
GPathogenic/Likely pathogenic