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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC8
(Y215C +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely pathogenic
HDAC8
(R166* +1 more)
Single nucleotide variant
(nonsense +1 more)
Inborn genetic diseases
+8 more
GPathogenic