List of variants reported as likely benign for familial restrictive cardiomyopathy by Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.360C>T (p.Ser120=)	rs150127220	0.00128
NM_000371.4(TTR):c.417G>A (p.Thr139=)	rs2276382	0.00104
NM_000371.4(TTR):c.337-14_337-11del	rs112263266

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