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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COG1, LOC130061576
(R55P)
Single nucleotide variant
(missense variant)
COG1 congenital disorder of glycosylation
GUncertain significance
COG1
(R187W)
Single nucleotide variant
(missense variant)
COG1 congenital disorder of glycosylation
GUncertain significance
COG1
(R571W)
Single nucleotide variant
(missense variant)
COG1 congenital disorder of glycosylation
GUncertain significance
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