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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2B
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
GRIN2B
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal dominant 6
+4 more
GBenign
GRIN2B
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal dominant 6
+4 more
GBenign
GRIN2B
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
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