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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRPF1
(R66C)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with dysmorphic facies and ptosis
GLikely benign
BRPF1
(R232W)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with dysmorphic facies and ptosis
GUncertain significance
BRPF1
(S394L)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with dysmorphic facies and ptosis
GUncertain significance
BRPF1
(N698S +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with dysmorphic facies and ptosis
GUncertain significance
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