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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYBPHL
(R232* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GUncertain significance
MYBPHL
(R201H +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance