List of variants in gene DCLRE1C reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.985T>A (p.Leu329Met)	rs41299658	0.00071
NM_001033855.3(DCLRE1C):c.419C>T (p.Ala140Val)	rs41297016	0.00054
NM_001033855.3(DCLRE1C):c.737C>T (p.Thr246Ile)	rs374596045	0.00005
NM_001033855.3(DCLRE1C):c.1834G>A (p.Val612Met)	rs751811224	0.00002
NM_001033855.3(DCLRE1C):c.350C>T (p.Pro117Leu)	rs757316102	0.00002
NM_001033855.3(DCLRE1C):c.1379AAG[2] (p.Glu462del)	rs373709012
NM_001033855.3(DCLRE1C):c.1732T>C (p.Tyr578His)	rs370816642
NM_001033855.3(DCLRE1C):c.1903dup (p.Ser635fs)	rs760288938

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