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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129933186, WDR35
(V869A +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
LOC129933186, WDR35
(V867F +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
LOC129933186, WDR35
(A852V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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