List of variants in gene DSP reported as uncertain significance for Hypertrophic cardiomyopathy

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.8014C>G (p.Gln2672Glu)	rs1064793890	0.00001
NM_004415.4(DSP):c.208A>G (p.Thr70Ala)	rs1442496444
NM_004415.4(DSP):c.4166G>A (p.Ser1389Asn)	rs763523853
NM_004415.4(DSP):c.5570A>C (p.Lys1857Thr)	rs1178938416

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