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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMK4
(D178N)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
CAMK4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CAMK4
(Q465R +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
CCDC69, CCNH
+385 more
Deletion
Familial adenomatous polyposis 1
+1 more
GPathogenic
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