List of variants in gene DDR2 reported as likely pathogenic for bone disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006182.4(DDR2):c.2255G>A (p.Arg752His)	rs1374086542	0.00001
NM_006182.4(DDR2):c.2323G>T (p.Val775Phe)	rs2102206250
NM_006182.4(DDR2):c.2516G>A (p.Arg839His)	rs1647819392

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