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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DVL3
(R580C)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 3
GUncertain significance
DVL3
(H650fs)
Microsatellite
(frameshift variant)
Autosomal dominant Robinow syndrome 3
GUncertain significance