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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL1A2
(G997S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta with normal sclerae, dominant form
+1 more
GPathogenic/Likely pathogenic
COL1A2
(G1030D)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
GUncertain significance