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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A37
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
ADAM28, ADAM7
+46 more
Copy number loss
not provided
GLikely pathogenic
ADAM28, ADAM7
+123 more
Copy number gain
not provided
GLikely pathogenic
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