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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADM
(K329E +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+7 more
GPathogenic/Likely pathogenic
SERPINF2, SGSM2
+25 more
Copy number loss
Lissencephaly
+2 more
GPathogenic