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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR81
(V349L)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
WDR81
(R756W)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GBenign/Likely benign
WDR81
(I1625M +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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