List of variants in gene VCL reported as benign by Ambry Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.2814C>G (p.Gly938=)	rs2131956	0.74148
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.339G>A (p.Arg113=)	rs56314318	0.06767
NM_014000.3(VCL):c.1407C>T (p.Ala469=)	rs2229507	0.06739
NM_014000.3(VCL):c.1506G>A (p.Arg502=)	rs2228373	0.06736
NM_014000.3(VCL):c.945C>A (p.Gly315=)	rs61731180	0.02850
NM_014000.3(VCL):c.2801C>T (p.Ala934Val)	rs16931179	0.00658
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.1671C>T (p.Asp557=)	rs137877092	0.00228
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.492T>G (p.Leu164=)	rs143702799	0.00033
NM_014000.3(VCL):c.1164C>T (p.Ile388=)	rs370852950	0.00003
NM_014000.3(VCL):c.1575A>C (p.Glu525Asp)	rs548487697
NM_014000.3(VCL):c.2560C>T (p.Leu854=)	rs551463686

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