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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PAPSS2
(R41*)
Single nucleotide variant
(nonsense)
Spondyloepimetaphyseal dysplasia, PAPSS2 type
+1 more
GPathogenic
PAPSS2
Single nucleotide variant
(splice donor variant)
Spondyloepimetaphyseal dysplasia, PAPSS2 type
GLikely pathogenic
PAPSS2
(E262K)
Single nucleotide variant
(missense variant)
Spondyloepimetaphyseal dysplasia, PAPSS2 type
GUncertain significance
PAPSS2
Single nucleotide variant
(splice donor variant)
Spondyloepimetaphyseal dysplasia, PAPSS2 type
GPathogenic
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