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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSRP3
Single nucleotide variant
(stop lost +1 more)
Hypertrophic cardiomyopathy 12
GUncertain significance
CSRP3
(R146C)
Single nucleotide variant
(synonymous variant +1 more)
Dilated cardiomyopathy 1M
+5 more
GUncertain significance
CSRP3
(S46R)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+5 more
GUncertain significance
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