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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC105370589, NRXN3
(K66E +2 more)
Single nucleotide variant
(missense variant +1 more)
Relative macrocephaly
+1 more
GPathogenic
NRXN3
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance