RS1064793527 COL1A2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
COL1A2-related disorder
Cardiovascular phenotype
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
COL1A2-related disorder
Cardiovascular phenotype
Other Variants in COL1A2