List of variants in gene DES reported as uncertain significance for Primary dilated 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_001927.4(DES):c.934G>A (p.Asp312Asn)	rs34337334	0.00059
NM_001927.4(DES):c.893C>T (p.Ser298Leu)	rs62636491	0.00014
NM_001927.4(DES):c.286G>T (p.Ala96Ser)	rs201190593	0.00001
NM_001927.4(DES):c.1234G>A (p.Glu412Lys)	rs869025380

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