List of variants in gene combination CAV3, OXTR reported as benign for 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_033337.3(CAV3):c.166G>A (p.Gly56Ser)	rs72546667	0.03558
NM_033337.3(CAV3):c.171G>A (p.Val57=)	rs61147808	0.01532
NM_033337.3(CAV3):c.233C>T (p.Thr78Met)	rs72546668	0.00302
NM_033337.3(CAV3):c.336C>T (p.Ile112=)	rs139985460	0.00157
NM_033337.3(CAV3):c.443G>A (p.Arg148Gln)	rs140575619	0.00049
NM_033337.3(CAV3):c.417C>T (p.Val139=)	rs147250678	0.00043
NM_033337.3(CAV3):c.204C>A (p.Ser68=)	rs116840775	0.00011

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