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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO39, FGF11
+209 more
Duplication
not provided
GUncertain significance
ACADVL, ACAP1
+62 more
Duplication
Very long chain acyl-CoA dehydrogenase deficiency
+1 more
GUncertain significance
ACADVL, ALOX12
+15 more
Deletion
Very long chain acyl-CoA dehydrogenase deficiency
GPathogenic
ACADVL, AIPL1
+22 more
Duplication
Developmental and epileptic encephalopathy, 25
GUncertain significance
DNAH2, DVL2
+81 more
Duplication
Common variable immunodeficiency
+1 more
GUncertain significance
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