List of variants in gene combination LOC126806068, RYR2 reported as benign for Catecholaminergic polymorphic ventricular tachycardia 1

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.13260+14A>G	rs141528541	0.00700
NM_001035.3(RYR2):c.12663C>T (p.Ser4221=)	rs370297602	0.00047
NM_001035.3(RYR2):c.12492G>A (p.Gln4164=)	rs377293019	0.00023
NM_001035.3(RYR2):c.12858C>T (p.Ser4286=)	rs185482345	0.00004
NM_001035.3(RYR2):c.12669G>A (p.Lys4223=)	rs147887477	0.00003
NM_001035.3(RYR2):c.12427A>C (p.Lys4143Gln)	rs750908017	0.00001
NM_001035.3(RYR2):c.12609G>T (p.Ala4203=)	rs372943408

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