List of variants in gene RYR2 reported as likely pathogenic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.7201C>T (p.Arg2401Cys)	rs1321283106	0.00004
NM_001035.3(RYR2):c.11934G>A (p.Met3978Ile)	rs794728826
NM_001035.3(RYR2):c.14288A>G (p.Asn4763Ser)	rs794728803
NM_001035.3(RYR2):c.7459_7470del (p.Leu2487_Val2490del)	rs1682404578

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