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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NT5E
(V278I)
Single nucleotide variant
(missense variant)
Hereditary arterial and articular multiple calcification syndrome
+2 more
GConflicting classifications of pathogenicity
NT5E
(A322V)
Single nucleotide variant
(missense variant)
Hereditary arterial and articular multiple calcification syndrome
GUncertain significance