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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAD
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CAD
(V1250M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CAD
(Q1798K +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
+1 more
GUncertain significance
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