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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX16
(F332del)
Deletion
(inframe_deletion +1 more)
Peroxisome biogenesis disorder 8B
GLikely pathogenic
PEX16
(R287C)
Single nucleotide variant
(missense variant)
Peroxisome biogenesis disorder 8A (Zellweger)
+3 more
GConflicting classifications of pathogenicity
PEX16
(D154G)
Single nucleotide variant
(missense variant)
Peroxisome biogenesis disorder 8A (Zellweger)
+5 more
GUncertain significance
PEX16
(S76L)
Single nucleotide variant
(missense variant)
Peroxisome biogenesis disorder 8A (Zellweger)
+1 more
GUncertain significance
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