List of variants in gene DYM reported as pathogenic for Smith-McCort dysplasia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001353214.3(DYM):c.621-2A>G	rs775414124	0.00001
NM_001353214.3(DYM):c.1789T>C (p.Cys597Arg)	rs120074165
NM_001353214.3(DYM):c.259G>A (p.Glu87Lys)	rs120074164

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