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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD5
(R308* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
+1 more
GPathogenic/Likely pathogenic
SETD5
(Y740C +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
SETD5
(S1188fs +1 more)
Duplication
(frameshift variant)
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
+2 more
GPathogenic/Likely pathogenic
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