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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRSF9
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CAMKK2, CCDC62
+73 more
Duplication
Deficiency of butyryl-CoA dehydrogenase
GUncertain significance