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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL1A1, LOC126862586
Single nucleotide variant
(intron variant)
Osteogenesis imperfecta type I
+1 more
GUncertain significance
COL1A1, LOC126862586
Duplication
not provided
+2 more
GPathogenic