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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
JAM3
Single nucleotide variant
(synonymous variant)
Porencephaly-microcephaly-bilateral congenital cataract syndrome
GUncertain significance
JAM3
(N241K +1 more)
Single nucleotide variant
(missense variant)
Porencephaly-microcephaly-bilateral congenital cataract syndrome
+1 more
GConflicting classifications of pathogenicity