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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR62
Single nucleotide variant
(splice donor variant)
Skraban-Deardorff syndrome
GLikely pathogenic
WDR62
(E526K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
WDR62
Single nucleotide variant
(intron variant)
Skraban-Deardorff syndrome
GUncertain significance
WDR62
(T1171M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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