ClinVar for MedGen (Select 1677486) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1397822	NM_006182.4(DDR2):c.2162A>G (p.Asn721Ser)	DDR2 (N721S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 932050	NM_006182.4(DDR2):c.1728+6T>C	DDR2	Single nucleotide variant (intron variant)	Warburg-cinotti syndrome +1 more	GUncertain significance
Select item 587365	NM_006182.4(DDR2):c.1829T>C (p.Leu610Pro)	DDR2 (L610P)	Single nucleotide variant (missense variant)	Warburg-cinotti syndrome	GPathogenic
Select item 586979	NM_006182.4(DDR2):c.2219A>G (p.Tyr740Cys)	DDR2 (Y740C)	Single nucleotide variant (missense variant)	Warburg-cinotti syndrome +1 more	GUncertain significance
Select item 259936	NM_006182.4(DDR2):c.83-39C>G	DDR2	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 259932	NM_006182.4(DDR2):c.1856+32G>T	DDR2	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 259930	NM_006182.4(DDR2):c.1504+25T>C	DDR2	Single nucleotide variant (intron variant)	Warburg-cinotti syndrome +3 more	GBenign
Select item 259929	NM_006182.4(DDR2):c.1260C>G (p.Leu420=)	DDR2	Single nucleotide variant (synonymous variant)	Warburg-cinotti syndrome +3 more	GBenign

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