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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2D
(S575L)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 46
+1 more
GConflicting classifications of pathogenicity
GRIN2D
(L677V)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 46
GLikely pathogenic
GRIN2D
Microsatellite
(inframe_insertion)
Developmental and epileptic encephalopathy, 46
GUncertain significance
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