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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DDX41
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DDX41
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
DDX41
(M1I)
Single nucleotide variant
(5 prime UTR variant +2 more)
DDX41-related hematologic malignancy predisposition syndrome
+2 more
GPathogenic/Likely pathogenic
ARL10, ARL14EPL
+511 more
Copy number gain
not provided
GLikely benign
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