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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPYSL3, STK32A
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DPYSL3, STK32A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
DPYSL3, STK32A
Single nucleotide variant
(intron variant)
not provided
GBenign
CCDC69, CCNH
+385 more
Deletion
Familial adenomatous polyposis 1
+1 more
GPathogenic
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