List of variants in gene DES reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.324G>A (p.Glu108=)	rs138677215	0.00189
NM_001927.4(DES):c.935A>C (p.Asp312Ala)	rs148947510	0.00093
NM_001927.4(DES):c.785A>T (p.Glu262Val)	rs147327878	0.00083
NM_001927.4(DES):c.924C>T (p.Asn308=)	rs578191306	0.00030
NM_001927.4(DES):c.1257C>T (p.Pro419=)	rs143154982	0.00013
NM_001927.4(DES):c.99C>T (p.Pro33=)	rs774006810	0.00006
NM_001927.4(DES):c.489G>A (p.Arg163=)	rs1448975712	0.00002
NM_001927.4(DES):c.402G>A (p.Ala134=)	rs369297392	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.1372-3dup	rs876657769
NM_001927.4(DES):c.578+10C>T	rs969392028
NM_001927.4(DES):c.736-3C>T
NM_001927.4(DES):c.897+4_897+5del	rs397516699
NM_001927.4(DES):c.898-37A>G
NM_001927.4(DES):c.898-38C>T

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