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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SON
(H527fs)
Deletion
(frameshift variant +2 more)
not provided
GPathogenic
SON
(A887T)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
SON
(V1734M)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
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