List of variants in gene DCLRE1C reported as likely 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.1008C>T (p.Asn336=)	rs115524993	0.00209
NC_000010.10:g.(14981869_14987103)_(14996432_?)dup
NM_001033855.3(DCLRE1C):c.1119A>C (p.Gly373=)	rs1554780259

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