List of variants in gene DES reported as likely benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.638C>T (p.Ala213Val)	rs41272699	0.01015
NM_001927.4(DES):c.18G>A (p.Ser6=)	rs199972656	0.00104
NM_001927.4(DES):c.665G>A (p.Arg222His)	rs367961979	0.00011
NM_001927.4(DES):c.1024-7C>G	rs779098835	0.00006
NM_001927.4(DES):c.195C>T (p.Gly65=)	rs1256584430	0.00001
NM_001927.4(DES):c.66G>A (p.Pro22=)	rs767502653	0.00001
NM_001927.4(DES):c.114G>A (p.Ala38=)	rs368901105
NM_001927.4(DES):c.1353C>T (p.Ile451=)	rs121913002
NM_001927.4(DES):c.735+14C>T	rs2125167702

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