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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NF2
Single nucleotide variant
(intron variant)
Familial meningioma
GUncertain significance
NF2
Single nucleotide variant
(splice donor variant +1 more)
Familial meningioma
GPathogenic
NF2
(R411H +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+5 more
GConflicting classifications of pathogenicity
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