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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DDOST
(R237H)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation type Ir
GUncertain significance
DDOST
(N191K)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation type Ir
+1 more
GUncertain significance