List of variants in gene CAPN3 reported as likely benign by Counsyl

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000070.3(CAPN3):c.2332G>A (p.Asp778Asn)	rs115311625	0.00908
NM_000070.3(CAPN3):c.2079A>G (p.Thr693=)	rs540561728	0.00005
NM_000070.3(CAPN3):c.2263+14A>G	rs886038225	0.00002
NM_000070.3(CAPN3):c.1914+13G>C	rs769337232
NM_000070.3(CAPN3):c.2088C>T (p.Ser696=)	rs867628179

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