List of variants in gene CSRP3 reported as uncertain significance for Dilated Cardiomyopathy, Dominant

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_003476.4(CSRP3):c.-181delC	rs886048102	0.00372
NM_003476.4(CSRP3):c.-161delG	rs138573509
NM_003476.4(CSRP3):c.-162_-161AG[6]	rs886048098
NM_003476.4(CSRP3):c.-180delA	rs34865888
NM_003476.4(CSRP3):c.-182delT	rs886048103

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