RS786201032 IFITM5
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type 5
IFITM5-related disorder
Osteogenesis imperfecta type 5
Osteogenesis imperfecta type 5
IFITM5-related disorder
Osteogenesis imperfecta type 5
Other Variants in IFITM5