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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRXN1
(V1412I +20 more)
Single nucleotide variant
(missense variant)
Pitt-Hopkins-like syndrome 2
GUncertain significance
NRXN1
(A10S)
Single nucleotide variant
(missense variant +1 more)
Pitt-Hopkins-like syndrome 2
GUncertain significance
NRXN1
(K286E)
Single nucleotide variant
(missense variant +1 more)
Pitt-Hopkins-like syndrome 2
GUncertain significance
NRXN1
(K260N)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
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