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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACVRL1
(R67W)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GPathogenic/Likely pathogenic
ACVRL1
(C308*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
ACVRL1
(V356M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GPathogenic/Likely pathogenic
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