ClinVar Miner

List of variants in gene CAPN3 reported as likely benign by Pars Genome Lab

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000070.3(CAPN3):c.897C>A (p.Leu299=)	rs370313391	0.00013
NM_000070.3(CAPN3):c.1947G>A (p.Glu649=)	rs79440238	0.00001

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