List of variants in gene VCL reported by Genetics and Genomics Program, Sidra Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.1907A>G (p.His636Arg)	rs71579374	0.00240
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg)	rs200342284
NM_014000.3(VCL):c.1575A>C (p.Glu525Asp)	rs548487697
NM_014000.3(VCL):c.1973T>C (p.Val658Ala)	rs372691803
NM_014000.3(VCL):c.2882C>A (p.Pro961Gln)	rs754591130

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