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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLFN12L
(T229S +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SLFN12L
(C67S +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
AP2B1, FNDC8
+13 more
Deletion
Peroxisome biogenesis disorder 3A (Zellweger)
GPathogenic
AP2B1, GAS2L2
+10 more
Duplication
Peroxisome biogenesis disorder 3A (Zellweger)
GUncertain significance
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