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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCG5, ABCG8
+443 more
Copy number gain
See cases
GPathogenic
SPTBN1, SPTBN1-AS1
(R44C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance