List of variants in gene DLL3 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_203486.3(DLL3):c.1674-10C>T	rs116099821	0.00950
NM_203486.3(DLL3):c.390G>A (p.Glu130=)	rs113780398	0.00200
NM_203486.3(DLL3):c.153C>T (p.Ser51=)	rs373980582	0.00061
NM_203486.3(DLL3):c.1758+57C>T	rs147582946	0.00024
NM_203486.3(DLL3):c.342C>T (p.Asp114=)	rs186303509	0.00019
NM_203486.3(DLL3):c.939G>A (p.Gly313=)	rs150100958	0.00016
NM_203486.3(DLL3):c.654G>T (p.Leu218=)	rs140489087	0.00006
NM_203486.3(DLL3):c.409+6T>C	rs995675341	0.00001
NM_203486.3(DLL3):c.1354G>A (p.Val452Ile)
NM_203486.3(DLL3):c.1449C>G (p.Leu483=)
NM_203486.3(DLL3):c.70-4C>T

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