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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKAP7, ARG1
+400 more
Deletion
Interstitial 6q microdeletion syndrome
GPathogenic
ENPP1
(R821H)
Single nucleotide variant
(missense variant)
Arterial calcification, generalized, of infancy, 1
+3 more
GConflicting classifications of pathogenicity