"PreventionGenetics, part of Exact Sciences"[submitter] AND "DMP1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 752888	NM_004407.4(DMP1):c.79T>C (p.Ser27Pro)	DMP1 (S27P)	Single nucleotide variant (missense variant)	DMP1-related disorder +1 more	GLikely benign
Select item 1049127	NM_004407.4(DMP1):c.293GAG[1] (p.Gly99del)	DMP1 (G83del +1 more)	Microsatellite (inframe_deletion)	DMP1-related disorder +1 more	GBenign/Likely benign
Select item 2051929	NM_004407.4(DMP1):c.421G>A (p.Asp141Asn)	DMP1 (D141N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3032115	NM_004407.4(DMP1):c.705A>G (p.Ala235=)	DMP1	Single nucleotide variant (synonymous variant)	DMP1-related disorder	GLikely benign
Select item 349978	NM_004407.4(DMP1):c.815G>A (p.Arg272His)	DMP1 (R272H +1 more)	Single nucleotide variant (missense variant)	DMP1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 732589	NM_004407.4(DMP1):c.997G>A (p.Val333Ile)	DMP1 (V317I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 349987	NM_004407.4(DMP1):c.1448A>C (p.Asn483Thr)	DMP1 (N483T +1 more)	Single nucleotide variant (missense variant)	DMP1-related disorder +2 more	GBenign

ClinVar