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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTR
(E74K)
Single nucleotide variant
(missense variant)
Familial amyloid neuropathy
+2 more
GPathogenic
TTR
(R124C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+9 more
GUncertain significance