List of variants in gene CAPN3 reported as likely benign for Autosomal recessive limb-girdle muscular dystrophy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000070.3(CAPN3):c.1800+21C>T	rs201512120	0.00156
NM_000070.3(CAPN3):c.329G>A (p.Arg110Gln)	rs188108732	0.00006
NM_000070.3(CAPN3):c.-25G>C	rs1405523432	0.00002

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