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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VNN2
(R340Q +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
VNN2
(T36I +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
VNN2
(S46F)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely benign
VNN2
(T17N)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
ARG1, CCN2
+19 more
Deletion
not provided
GPathogenic
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