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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PGAP2
(T49I +4 more)
Single nucleotide variant
(missense variant +4 more)
Hyperphosphatasia with intellectual disability syndrome 3
+1 more
GConflicting classifications of pathogenicity
PGAP2
(Y99C +6 more)
Single nucleotide variant
(missense variant +3 more)
Hyperphosphatasia with intellectual disability syndrome 3
GPathogenic
PGAP2
(R181L +8 more)
Single nucleotide variant
(missense variant +2 more)
Hyperphosphatasia with intellectual disability syndrome 3
GLikely pathogenic
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