ClinVar Miner

List of variants in gene VCL studied for Primary familial hypertrophic cardiomyopathy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.1907A>G (p.His636Arg)	rs71579374	0.00145
NM_014000.3(VCL):c.2468G>A (p.Arg823Gln)	rs759202535	0.00006
NM_014000.3(VCL):c.2923C>T (p.Arg975Trp)	rs121917776	0.00001

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