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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13B
(T1869M +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
VPS13B
(N2139S +1 more)
Single nucleotide variant
(missense variant)
Cohen syndrome
+4 more
GConflicting classifications of pathogenicity
VPS13B
(C2709Y +1 more)
Single nucleotide variant
(missense variant)
Cohen syndrome
GUncertain significance
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