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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECOM
(R750W +8 more)
Single nucleotide variant
(missense variant)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GConflicting classifications of pathogenicity
MECOM
(H235P +3 more)
Single nucleotide variant
(missense variant +1 more)
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
GUncertain significance