RS876661151 GRIN2B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 6
Developmental and epileptic encephalopathy
27
Joint hypermobility
Motor delay
Delayed speech and language development
Astigmatism
Long fingers
Developmental and epileptic encephalopathy
27
Intellectual disability
autosomal dominant 6
Intellectual disability
autosomal dominant 6
Other Variants in GRIN2B