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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL1A2
(G109V)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta, perinatal lethal
GLikely pathogenic
COL1A2
(G199D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GLikely pathogenic
COL1A2
(G256V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
COL1A2
(G358S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type III
+9 more
GPathogenic
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