List of variants in gene CAPN3 reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000070.3(CAPN3):c.96T>C (p.Thr32=)	rs1801496	0.09551
NM_000070.3(CAPN3):c.606T>C (p.Ser202=)	rs17593	0.05293
NM_000070.3(CAPN3):c.2380+12del	rs28364538	0.04623
NM_000070.3(CAPN3):c.1029+3A>G	rs28364442	0.03285
NM_000070.3(CAPN3):c.78G>A (p.Pro26=)	rs62642519	0.01774
NM_000070.3(CAPN3):c.62G>A (p.Gly21Glu)	rs28364364	0.01193
NM_000070.3(CAPN3):c.2433T>C (p.Val811=)	rs28364543	0.01154
NM_000070.3(CAPN3):c.1116-5A>G	rs28364467	0.01144
NM_000070.3(CAPN3):c.2332G>A (p.Asp778Asn)	rs115311625	0.00908
NM_000070.3(CAPN3):c.73C>T (p.His25Tyr)	rs61735534	0.00885
NM_000070.3(CAPN3):c.984C>T (p.Cys328=)	rs28364441	0.00600
NM_000070.3(CAPN3):c.2381-12A>G	rs73402734	0.00578
NM_000070.3(CAPN3):c.318C>T (p.Cys106=)	rs117609395	0.00495

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