List of variants in gene combination LOC126806067, RYR2 reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 2

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.4068C>T (p.Pro1356=)	rs199821105	0.00240
NM_001035.3(RYR2):c.4069G>C (p.Asp1357His)	rs193922626	0.00010
NM_001035.3(RYR2):c.4094C>T (p.Ala1365Val)	rs373261115	0.00010
NM_001035.3(RYR2):c.4044G>A (p.Lys1348=)	rs755391572	0.00009
NM_001035.3(RYR2):c.3823G>A (p.Gly1275Ser)	rs769294223	0.00001
NM_001035.3(RYR2):c.3766C>A (p.Pro1256Thr)	rs769729405

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