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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ETFB
(V79I)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign/Likely benign
ETFB
(R47del)
Deletion
(inframe_deletion +1 more)
Multiple acyl-CoA dehydrogenase deficiency
GUncertain significance
ETFB
(E40A)
Single nucleotide variant
(missense variant +1 more)
Multiple acyl-CoA dehydrogenase deficiency
+3 more
GBenign/Likely benign
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