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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX26
(N67S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
PEX26
Single nucleotide variant
(synonymous variant)
Peroxisome biogenesis disorder 7A (Zellweger)
+2 more
GBenign/Likely benign
PEX26
(R191W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
PEX26
(R191Q)
Single nucleotide variant
(missense variant)
Peroxisome biogenesis disorder 7A (Zellweger)
+1 more
GUncertain significance
PEX26
(L239P)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
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