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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNT10A
(C107*)
Single nucleotide variant
(nonsense)
not provided
+6 more
GPathogenic
WNT10A
(F228I)
Single nucleotide variant
(missense variant)
SchC6pf-Schulz-Passarge syndrome
+7 more
GConflicting classifications of pathogenicity