List of variants in gene VCL reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.2814C>G (p.Gly938=)	rs2131956	0.73000
NM_014000.3(VCL):c.875-24T>A	rs1908339	0.65590
NM_014000.3(VCL):c.2388G>A (p.Pro796=)	rs767809	0.42862
NM_014000.3(VCL):c.768T>C (p.Asp256=)	rs56413529	0.06776
NM_014000.3(VCL):c.1407C>T (p.Ala469=)	rs2229507	0.06287
NM_014000.3(VCL):c.945C>A (p.Gly315=)	rs61731180	0.02850
NM_014000.3(VCL):c.2950-22C>G	rs71579378	0.00753
NM_014000.3(VCL):c.1557C>A (p.Ile519=)	rs150120464	0.00466
NM_014000.3(VCL):c.1317T>C (p.Ser439=)	rs71579355	0.00442
NM_014000.3(VCL):c.623-30A>G	rs200699818	0.00258
NM_014000.3(VCL):c.2025G>A (p.Val675=)	rs140766884	0.00256
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.3333T>C (p.Ala1111=)	rs147415627	0.00019

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