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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPV4
(P692L +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+6 more
GPathogenic
TRPV4
(E690K +3 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic