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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA2
Single nucleotide variant
(splice donor variant)
Nicolaides-Baraitser syndrome
+1 more
GUncertain significance
SMARCA2
(G92R)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GUncertain significance
SMARCA2
(G752R)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
+1 more
GLikely pathogenic
SMARCA2
(T756I)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
+1 more
GUncertain significance
SMARCA2
(S783L)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
+2 more
GConflicting classifications of pathogenicity
SMARCA2
(N787K)
Single nucleotide variant
(missense variant)
SMARCA2-related BAFopathy
+1 more
GConflicting classifications of pathogenicity
SMARCA2
(P883L)
Single nucleotide variant
(missense variant +1 more)
SMARCA2-related BAFopathy
+2 more
GPathogenic
SMARCA2
(R879H +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
SMARCA2
(R1047H +1 more)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
+2 more
GConflicting classifications of pathogenicity
SMARCA2
(P1092A +1 more)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GUncertain significance
SMARCA2
(R1159Q +1 more)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
+2 more
GPathogenic/Likely pathogenic
SMARCA2
(V1566I +5 more)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GUncertain significance
SMARCA2
(F228L +5 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SMARCA2
(D1589H +5 more)
Single nucleotide variant
(missense variant)
Nicolaides-Baraitser syndrome
GUncertain significance
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