List of variants in gene CSRP3 reported as likely pathogenic for Primary dilated cardiomyopathy

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: 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.354G>A (p.Glu118=)	rs876657767
NM_003476.5(CSRP3):c.46A>T (p.Thr16Ser)	rs1565053147
NM_003476.5(CSRP3):c.96G>A (p.Lys32=)	rs1565053085

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