List of variants in gene VCL reported as likely benign by PreventionGenetics, part of Exact Sciences

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.2025G>A (p.Val675=)	rs140766884	0.00256
NM_014000.3(VCL):c.1907A>G (p.His636Arg)	rs71579374	0.00240
NM_014000.3(VCL):c.1572C>T (p.Ala524=)	rs138566234	0.00086
NM_014000.3(VCL):c.492T>G (p.Leu164=)	rs143702799	0.00033
NM_014000.3(VCL):c.1788A>C (p.Ser596=)	rs199582103	0.00021
NM_014000.3(VCL):c.590C>T (p.Thr197Ile)	rs189242810	0.00019
NM_014000.3(VCL):c.2142C>T (p.Asp714=)	rs373790383	0.00009
NM_014000.3(VCL):c.3066C>T (p.Ile1022=)	rs138619320	0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=)	rs147415627	0.00008
NM_014000.3(VCL):c.404T>C (p.Ile135Thr)	rs373744314	0.00006
NM_014000.3(VCL):c.2028C>G (p.Val676=)	rs528539468	0.00004
NM_014000.3(VCL):c.1170T>C (p.Ala390=)	rs201459260	0.00002
NM_014000.3(VCL):c.3381T>C (p.Val1127=)	rs943734765	0.00001
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg)	rs200342284
NM_014000.3(VCL):c.2091C>A (p.Thr697=)	rs775493699
NM_014000.3(VCL):c.2560C>T (p.Leu854=)	rs551463686

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