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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPH2, LOC126805726
(R125C +4 more)
Single nucleotide variant
(missense variant +1 more)
Ventricular septal defect
+3 more
GConflicting classifications of pathogenicity
DPH2, LOC126805726
(Q115* +5 more)
Single nucleotide variant
(nonsense +1 more)
Ventricular septal defect
+3 more
GConflicting classifications of pathogenicity