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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPP6
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal dominant 33
GUncertain significance
DPP6
(K159R +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
DPP6
(I218M +4 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 33
GUncertain significance
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