List of variants in gene DCLRE1C reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.1991G>A (p.Arg664Gln)	rs779159378	0.00004
NM_001033855.3(DCLRE1C):c.380A>G (p.Asn127Ser)	rs752558172	0.00004
NM_001033855.3(DCLRE1C):c.1825G>T (p.Asp609Tyr)
NM_001033855.3(DCLRE1C):c.1903dup (p.Ser635fs)	rs760288938
NM_001033855.3(DCLRE1C):c.869C>T (p.Ser290Phe)

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