List of variants in gene DCLRE1C reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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.265A>G (p.Thr89Ala)	rs756366535	0.00003
NM_001033855.3(DCLRE1C):c.475A>T (p.Ile159Phe)	rs757929355	0.00001

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