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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NT5E
(T376A)
Single nucleotide variant
(missense variant)
Hereditary arterial and articular multiple calcification syndrome
GBenign
NT5E
Single nucleotide variant
(intron variant)
Hereditary arterial and articular multiple calcification syndrome
GBenign