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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2D, LOC130064855
(A67T)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 46
GLikely benign
GRIN2D
(G226R)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
GRIN2D
(R798P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
GRIN2D
(S917G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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