List of variants in gene DES reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.75A>G (p.Pro25=)	rs1318299	0.89847
NM_001927.4(DES):c.93T>C (p.Ser31=)	rs2017800	0.88201
NM_001927.4(DES):c.578+11G>A	rs111548596	0.06130
NM_001927.4(DES):c.669T>C (p.Ile223=)	rs75882680	0.02876
NM_001927.4(DES):c.638C>T (p.Ala213Val)	rs41272699	0.01015
NM_001927.4(DES):c.324G>A (p.Glu108=)	rs138677215	0.00189
NM_001927.4(DES):c.792C>T (p.Asp264=)	rs150370918	0.00168
NM_001927.4(DES):c.18G>A (p.Ser6=)	rs199972656	0.00104
NM_001927.4(DES):c.924C>T (p.Asn308=)	rs578191306	0.00030
NM_001927.4(DES):c.736-8C>A	rs140375681	0.00021
NM_001927.4(DES):c.897+16C>T	rs370385097	0.00011
NM_001927.4(DES):c.736-19G>A	rs745667526	0.00009
NM_001927.4(DES):c.114G>A (p.Ala38=)	rs368901105
NM_001927.4(DES):c.897+4_897+5del	rs397516699

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