List of variants in gene DCLRE1C reported as likely benign by GeneDx

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.1284A>C (p.Lys428Asn)	rs113870881	0.00202
NM_001033855.3(DCLRE1C):c.*4T>C	rs377639023	0.00101
NM_001033855.3(DCLRE1C):c.1894G>A (p.Glu632Lys)	rs61757205	0.00024

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