List of variants reported as uncertain significance for Ehlers-Danlos syndrome, classic type; Osteogenesis imperfecta type I

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000089.4(COL1A2):c.1976A>G (p.Glu659Gly)	rs766488808	0.00002
NC_000007.14:g.(?_94395022)_(94585525_?)dup
NM_000089.4(COL1A2):c.2148_2156delinsACGTGG (p.Val717_Pro719delinsArgGly)	rs1584326175

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