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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130062906, LOC130062907
+222 more
Copy number loss
See cases
GPathogenic
APC2, LOC130062956
Single nucleotide variant
(synonymous variant)
not provided
GBenign
APC2, LOC130062956
(A1912V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
APC2, LOC130062956
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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