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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PHF7
Duplication
(splice acceptor variant)
not provided
+1 more
GBenign/Likely benign
PHF7
(N336H +1 more)
Single nucleotide variant
(missense variant)
PHF7-related disorder
GLikely benign