List of variants in gene DES reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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.170C>T (p.Ser57Leu)	rs372825868	0.00077
NM_001927.4(DES):c.365A>G (p.Tyr122Cys)	rs1400593451
NM_001927.4(DES):c.404C>T (p.Ala135Val)	rs546741834
NM_001927.4(DES):c.709G>A (p.Ala237Thr)	rs397516697

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