List of variants in gene DYM reported as uncertain significance by GeneDx

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_001353214.3(DYM):c.316G>A (p.Ala106Thr)	rs150635814	0.00014
NM_001353214.3(DYM):c.1924T>C (p.Phe642Leu)	rs151034190	0.00011
NM_001353214.3(DYM):c.1849G>A (p.Asp617Asn)	rs769667648	0.00001
NM_001353214.3(DYM):c.934A>G (p.Lys312Glu)	rs2145831177

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