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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYNC2H1
(G1974*)
Single nucleotide variant
(nonsense)
Heart, malformation of
+4 more
GLikely pathogenic
DYNC2H1
(I3303T +1 more)
Single nucleotide variant
(missense variant)
Heart, malformation of
+4 more
GUncertain significance