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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA2
(W795R)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GPathogenic
SMARCA2
(H854L)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GPathogenic
SMARCA2
(A1201V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
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