ClinVar Miner

List of variants in gene VCL reported as pathogenic for Hypertrophic cardiomyopathy 15

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.829C>A (p.Leu277Met)	rs71579353	0.00010
NM_014000.3(VCL):c.2923C>T (p.Arg975Trp)	rs121917776	0.00001

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