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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SON
(P1214S)
Single nucleotide variant
(missense variant +2 more)
ZTTK syndrome
+1 more
GLikely benign
SON
(H1528R)
Single nucleotide variant
(missense variant +2 more)
ZTTK syndrome
+1 more
GBenign/Likely benign
SON
(S1595P)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GConflicting classifications of pathogenicity
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