List of variants in gene VCL reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.688C>T (p.Arg230Cys)	rs139312390	0.00010
NM_014000.3(VCL):c.2467C>T (p.Arg823Trp)	rs779047174	0.00006
NM_014000.3(VCL):c.2468G>A (p.Arg823Gln)	rs759202535	0.00006
NM_014000.3(VCL):c.1940C>T (p.Ala647Val)	rs534449109	0.00003
NM_014000.3(VCL):c.1558C>T (p.Arg520Trp)	rs377722209	0.00002
NM_014000.3(VCL):c.592G>A (p.Val198Met)	rs760340545	0.00001
NM_014000.3(VCL):c.689G>A (p.Arg230His)	rs749628307	0.00001
NM_014000.3(VCL):c.1820A>G (p.Lys607Arg)	rs2131918378
NM_014000.3(VCL):c.2276G>A (p.Arg759Gln)	rs1425397914
NM_014000.3(VCL):c.2692A>G (p.Met898Val)	rs2131933674
NM_014000.3(VCL):c.379G>A (p.Asp127Asn)	rs1554816666

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