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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALPL
(R136H +2 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
WNT1
(G252R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
WNT1
(C330Y)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta
GUncertain significance
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