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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADCYAP1, AFG3L2
+367 more
Copy number loss
Deletion of short arm of chromosome 18
GPathogenic
LPIN2
(K387E)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome
+4 more
GBenign/Likely benign