ClinVar Miner

List of variants in gene RYR2 reported as benign for Arrhythmogenic right ventricular dysplasia 2

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Total variants: 43
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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.*1140A>G rs12594 0.28188
NM_001035.3(RYR2):c.*1307C>T rs16835904 0.16356
NM_001035.3(RYR2):c.849-8T>C rs16835237 0.09863
NM_001035.3(RYR2):c.1611G>A (p.Leu537=) rs78281932 0.05734
NM_001035.3(RYR2):c.4684-11C>T rs7546045 0.05719
NM_001035.3(RYR2):c.5400A>G (p.Lys1800=) rs3820216 0.03524
NM_001035.3(RYR2):c.1776A>T (p.Gly592=) rs72549414 0.02926
NM_001035.3(RYR2):c.9449+8T>A rs60777199 0.02348
NM_001035.3(RYR2):c.*56C>A rs74703306 0.01808
NM_001035.3(RYR2):c.*328C>T rs76286925 0.01804
NM_001035.3(RYR2):c.5654G>A (p.Gly1885Glu) rs41315858 0.01767
NM_001035.3(RYR2):c.14421C>T (p.Asp4807=) rs75206601 0.01733
NM_001035.3(RYR2):c.6928+4G>A rs79862521 0.01335
NM_001035.3(RYR2):c.4684-5G>C rs7522981 0.01334
NM_001035.3(RYR2):c.2397-6C>T rs78165942 0.01029
NM_001035.3(RYR2):c.8448C>T (p.Asp2816=) rs144876996 0.00659
NM_001035.3(RYR2):c.4740G>A (p.Pro1580=) rs79811945 0.00119
NM_001035.3(RYR2):c.649A>G (p.Ile217Val) rs200642525 0.00029
NM_001035.3(RYR2):c.*129C>G rs16835891
NM_001035.3(RYR2):c.*714C>G rs12406863
NM_001035.3(RYR2):c.1477-11del rs397516518
NM_001035.3(RYR2):c.9318T>G (p.Ser3106=) rs2797436

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