List of variants in gene RYR2 reported as benign for Cardiac arrhythmia

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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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.10935+18C>T	rs2797445	0.98361
NM_001035.3(RYR2):c.6906T>C (p.Leu2302=)	rs707189	0.96110
NM_001035.3(RYR2):c.10776C>T (p.Ser3592=)	rs2685301	0.95962
NM_001035.3(RYR2):c.10503C>T (p.Thr3501=)	rs2797441	0.95950
NM_001035.3(RYR2):c.3423+49A>G	rs2805390	0.90629
NM_001035.3(RYR2):c.2973A>G (p.Ser991=)	rs2253273	0.84980
NM_001035.3(RYR2):c.11326-23C>T	rs2253831	0.73062
NM_001035.3(RYR2):c.2718+26A>G	rs2618702	0.71570
NM_001035.3(RYR2):c.13783-6A>G	rs790901	0.66919
NM_001035.3(RYR2):c.13913+12A>C	rs790900	0.66578
NM_001035.3(RYR2):c.13783-21G>A	rs790902	0.64306
NM_001035.3(RYR2):c.13476+16A>G	rs2256242	0.60593
NM_001035.3(RYR2):c.677-11T>A	rs10754602	0.53281
NM_001035.3(RYR2):c.1359C>T (p.Ser453=)	rs3765097	0.51474
NM_001035.3(RYR2):c.1612+14T>C	rs2045955	0.48321
NM_001035.3(RYR2):c.7806C>T (p.His2602=)	rs684923	0.47802
NM_001035.3(RYR2):c.6556-41G>A	rs10802626	0.39733
NM_001035.3(RYR2):c.14091-25G>A	rs9428384	0.37110
NM_001035.3(RYR2):c.11963-11T>C	rs790889	0.35417
NM_001035.3(RYR2):c.13476+47G>A	rs16835818	0.34821
NM_001035.3(RYR2):c.464-8A>C	rs10925391	0.33866
NM_001035.3(RYR2):c.7488C>T (p.Leu2496=)	rs143906555	0.00397
NM_001035.3(RYR2):c.5586C>T (p.Asp1862=)	rs193922628	0.00123
NM_001035.3(RYR2):c.1477-11del	rs397516518
NM_001035.3(RYR2):c.9318T>G (p.Ser3106=)	rs2797436

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