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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRDM16
(D236N)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 8
+1 more
GLikely benign
PRDM16
(P548T)
Single nucleotide variant
(missense variant)
Wolff-Parkinson-White pattern
GUncertain significance
PRDM16
(P889L)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 8
+2 more
GUncertain significance
PRDM16
(T952M)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 8
GUncertain significance
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