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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX19
(Q176E)
Single nucleotide variant
(missense variant +1 more)
Peroxisome biogenesis disorder 12A (Zellweger)
GUncertain significance
PEX19
(S9G)
Single nucleotide variant
(missense variant +1 more)
Peroxisome biogenesis disorder 12A (Zellweger)
GUncertain significance
PEX19
(E6K)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
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