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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A22
(E221del)
Microsatellite
(inframe_deletion)
Developmental and epileptic encephalopathy, 3
GUncertain significance
SLC25A22
(G64S)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 3
+3 more
GUncertain significance
C11orf40, C11orf42
+243 more
Copy number gain
Silver-Russell syndrome 1
GPathogenic
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