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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPP6
Single nucleotide variant
(intron variant)
Ventricular fibrillation, paroxysmal familial, 2
+1 more
GPathogenic; risk factor
DPP6
Single nucleotide variant
(synonymous variant +2 more)
not provided
GBenign
DPP6
Single nucleotide variant
(intron variant +2 more)
Intellectual disability, autosomal dominant 33
+1 more
GBenign
DPP6
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
DPP6
Single nucleotide variant
(intron variant)
not specified
GBenign
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