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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADS
(R107C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GPathogenic
ACADS
(R171W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign/Likely benign
ACADS
(G209S +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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