List of variants in gene COL1A2 reported as uncertain significance for Ehlers-Danlos syndrome, classic type; Osteogenesis imperfecta type I

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000089.4(COL1A2):c.1976A>G (p.Glu659Gly)	rs766488808	0.00002
NM_000089.4(COL1A2):c.2148_2156delinsACGTGG (p.Val717_Pro719delinsArgGly)	rs1584326175

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