RS755058199 COL1A2

Health Risk Chr 7:94412602
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Associated Conditions
Autosomal dominant COL1A2-related disorders
Ehlers-Danlos syndrome
Osteogenesis imperfecta type I
classic type
1
Cardiovascular phenotype
Autosomal dominant COL1A2-related disorders
Ehlers-Danlos syndrome
Osteogenesis imperfecta type I
classic type
1
Cardiovascular phenotype
Other Variants in COL1A2
rs72656357 rs72659319 rs72659345 rs74315146 rs121912900 rs121912901 rs121912902 rs121912903 rs121912904 rs121912905
Ask Dr. Hemsworth about this variant