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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
JMJD7, JMJD7-PLA2G4B
+1 more
(P17L)
Single nucleotide variant
(missense variant)
not provided
GBenign
JMJD7, JMJD7-PLA2G4B
(A28G)
Single nucleotide variant
(missense variant)
not provided
GBenign
JMJD7, JMJD7-PLA2G4B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CGNL1, MAPDA
+472 more
Duplication
Familial colorectal cancer
+1 more
GUncertain significance
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