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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13B
(P1088A)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
VPS13B
(S1516fs +1 more)
Deletion
(frameshift variant)
Progressive visual loss
+9 more
GPathogenic
VPS13B
(Y3111fs +1 more)
Insertion
(frameshift variant)
Cohen syndrome
GBenign
VPS13B
(Q3772* +1 more)
Single nucleotide variant
(nonsense)
not provided
+10 more
GPathogenic
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