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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCOM1, POLR2M
(R461C +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
GCOM1, POLR2M
(D544N +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
CGNL1, MAPDA
+472 more
Duplication
Familial colorectal cancer
+1 more
GUncertain significance
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