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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNT1
(S88R)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta
+4 more
GBenign/Likely benign
WNT1
(G169C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WNT1
(G222R)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
WNT1
(T336fs)
Deletion
(frameshift variant)
not provided
GPathogenic/Likely pathogenic
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