List of variants in gene DCLRE1C reported as uncertain significance by Genome-Nilou Lab

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001033855.3(DCLRE1C):c.169G>T (p.Val57Phe)	rs138077101	0.00016
NM_001033855.3(DCLRE1C):c.1385A>T (p.Glu462Val)	rs115250914	0.00015
NM_001033855.3(DCLRE1C):c.456C>T (p.Ser152=)	rs140176235	0.00005
NM_001033855.3(DCLRE1C):c.1898A>G (p.Glu633Gly)	rs533771936	0.00002
NM_001033855.3(DCLRE1C):c.1249T>G (p.Ser417Ala)	rs1013537366
NM_001033855.3(DCLRE1C):c.17G>A (p.Gly6Glu)	rs2131239353
NM_001033855.3(DCLRE1C):c.1903dup (p.Ser635fs)	rs760288938

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