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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HADH
(L86P +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
HADH
Single nucleotide variant
(synonymous variant)
Deficiency of 3-hydroxyacyl-CoA dehydrogenase
+2 more
GConflicting classifications of pathogenicity