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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRWD3
(M1736L)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(T1595I)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(R1529Q)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
+1 more
GUncertain significance
BRWD3
(G1342E)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(Y1040C)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(S893F)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(R699*)
Single nucleotide variant
(nonsense)
Intellectual disability, X-linked 93
GLikely pathogenic
BRWD3
Single nucleotide variant
(splice acceptor variant)
Intellectual disability, X-linked 93
GLikely pathogenic
BRWD3
(G290E)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
BRWD3
(D84H)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
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