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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSRP1
(Q18*)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
NSRP1
(K371fs +1 more)
Duplication
(frameshift variant)
Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities
+4 more
GPathogenic
NSRP1
(E401fs +1 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities
+4 more
GPathogenic
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