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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRXN1
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GLikely benign
NRXN1
(P469S +7 more)
Single nucleotide variant
(missense variant)
Pitt-Hopkins-like syndrome 2
+4 more
GBenign/Likely benign