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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13B
(C1117fs)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic
VPS13B
(I2795T)
Single nucleotide variant
(missense variant)
Cohen syndrome
+1 more
GUncertain significance
VPS13B
(L3062fs +1 more)
Duplication
(frameshift variant)
Inborn genetic diseases
+1 more
GPathogenic
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