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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRXN2
(D1412fs +2 more)
Deletion
(frameshift variant +1 more)
not provided
GUncertain significance
NRXN2
(V799L +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NRXN2
(G599S +4 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NRXN2
(S410P +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NRXN2
(E30A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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