List of variants in gene VCL reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.875-24T>A	rs1908339	0.65590
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.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.1177-15C>T	rs115083446	0.00414
NM_014000.3(VCL):c.1542C>T (p.Val514=)	rs7904077	0.00380
NM_014000.3(VCL):c.2025G>A (p.Val675=)	rs140766884	0.00256
NM_014000.3(VCL):c.2023-20A>G	rs143756084	0.00247
NM_014000.3(VCL):c.1671C>T (p.Asp557=)	rs137877092	0.00228
NM_014000.3(VCL):c.2434+19T>C	rs188216596	0.00198
NM_014000.3(VCL):c.1353-19G>A	rs145537824	0.00193
NM_014000.3(VCL):c.660C>T (p.Asn220=)	rs56264452	0.00091
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.1626C>T (p.Leu542=)	rs150402791	0.00031
NM_014000.3(VCL):c.622+4C>T	rs201020802

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