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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARRDC3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ARRDC3
Single nucleotide variant
(5 prime UTR variant +3 more)
not provided
GBenign
LUCAT1, ADGRV1
+1 more
Deletion
not provided
GLikely pathogenic
ARAP3, CCDC69
+385 more
Deletion
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
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