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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRWD1
(C161fs)
Deletion
(frameshift variant)
Ciliary dyskinesia, primary, 51
GUncertain significance
BRWD1
(E973G)
Single nucleotide variant
(missense variant)
Ciliary dyskinesia, primary, 51
GUncertain significance
BRWD1
(Q1858L)
Single nucleotide variant
(missense variant)
Ciliary dyskinesia, primary, 51
+5 more
GPathogenic/Likely pathogenic
BRWD1
(H175Y)
Single nucleotide variant
(missense variant)
Ciliary dyskinesia, primary, 51
+5 more
GConflicting classifications of pathogenicity
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