List of variants in gene CSRP3 reported as benign for Cardiomyopathy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003476.5(CSRP3):c.336G>A (p.Ala112=)	rs13451	0.07238
NM_003476.5(CSRP3):c.312C>G (p.Thr104=)	rs45582433	0.01721
NM_003476.5(CSRP3):c.213C>T (p.Ile71=)	rs45476991	0.00466
NM_003476.5(CSRP3):c.299G>A (p.Arg100His)	rs138218523	0.00091

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