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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSRP3
(R146H +1 more)
Single nucleotide variant
(missense variant)
Prolonged QT interval
+5 more
GUncertain significance
CSRP3
(R64L)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
GUncertain significance
CSRP3
(L44P)
Single nucleotide variant
(missense variant +1 more)
See cases
+6 more
GConflicting classifications of pathogenicity
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