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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCCB
(L17M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
PCCB
(L28V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
PCCB
(R113Q)
Single nucleotide variant
(missense variant)
Propionic acidemia
+2 more
GConflicting classifications of pathogenicity
PCCB
(A497V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
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