List of variants reported as pathogenic for Osteogenesis imperfecta type 10

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.75554407_75559680del
NM_001235.5(SERPINH1):c.1233dup (p.Asp412Ter)	rs1565244847
NM_001235.5(SERPINH1):c.233T>C (p.Leu78Pro)	rs137853892
NM_001235.5(SERPINH1):c.710T>C (p.Met237Thr)	rs886039819

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