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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD17B4, LOC129994460
(G16S)
Single nucleotide variant
(missense variant +1 more)
Bifunctional peroxisomal enzyme deficiency
+4 more
GConflicting classifications of pathogenicity
HSD17B4
(I307T +8 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HSD17B4
(A491T +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign/Likely benign
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