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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNT5A
(C139F +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 1
GUncertain significance
WNT5A
(C69Y +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 1
GUncertain significance