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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS33B
(R567G +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
VPS33B
(P164R +2 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, renal dysfunction, and cholestasis 1
GUncertain significance
VPS33B
(F15S)
Single nucleotide variant
(missense variant +1 more)
Arthrogryposis, renal dysfunction, and cholestasis 1
GUncertain significance
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