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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRWD3
Microsatellite
(intron variant)
not provided
+1 more
GBenign
BRWD3
Single nucleotide variant
(intron variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
BRWD3
(L564F)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
GUncertain significance
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