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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSRP3
(R76S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CSRP3
(G72R)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GUncertain significance
CSRP3
(M1T)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely pathogenic
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