List of variants in gene CSRP3 reported as benign for cardiomyopathy

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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: 11

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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.*629T>C	rs45599440	0.06866
NM_003476.5(CSRP3):c.150G>A (p.Ala50=)	rs7124801	0.03207
NM_003476.5(CSRP3):c.312C>G (p.Thr104=)	rs45582433	0.01721
NM_003476.5(CSRP3):c.213C>T (p.Ile71=)	rs45476991	0.00499
NM_003476.5(CSRP3):c.508+18C>T	rs144404101	0.00332
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg)	rs45550635	0.00271
NM_003476.5(CSRP3):c.162G>A (p.Ser54=)	rs112848043	0.00104
NM_003476.5(CSRP3):c.299G>A (p.Arg100His)	rs138218523	0.00097
NM_003476.5(CSRP3):c.327A>G (p.Lys109=)	rs778512127	0.00003
NM_003476.5(CSRP3):c.508+9T>C	rs727504517

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