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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HAND2, HAND2-AS1
(G93W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AADAT, ACSL1
+68 more
Copy number loss
not provided
GPathogenic
SPATA18, SPATA4
+537 more
Copy number gain
not provided
GPathogenic
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