List of variants reported as likely pathogenic for Osteogenesis imperfecta type I by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000088.4(COL1A1):c.1461+2T>G	rs1907417140
NM_000088.4(COL1A1):c.3128G>C (p.Gly1043Ala)	rs1906767501
NM_000088.4(COL1A1):c.3360del (p.Gly1121fs)	rs1260429820
NM_000088.4(COL1A1):c.904-1G>C	rs1907593112

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