List of variants in gene VCAN reported as likely benign for not specified

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004385.5(VCAN):c.6237G>A (p.Lys2079=)	rs80200229	0.01278
NM_004385.5(VCAN):c.5187G>A (p.Glu1729=)	rs35648048	0.00302
NM_004385.5(VCAN):c.574G>A (p.Gly192Arg)	rs141008923	0.00245
NM_004385.5(VCAN):c.5750A>T (p.Tyr1917Phe)	rs141477510	0.00225
NM_004385.5(VCAN):c.3713G>C (p.Arg1238Thr)	rs146560021	0.00071
NM_004385.5(VCAN):c.2234A>C (p.Lys745Thr)	rs144502710	0.00018
NM_004385.5(VCAN):c.9454C>G (p.Leu3152Val)	rs183984308	0.00007

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