ClinVar Miner

List of variants in gene RYR2 reported as benign by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 46
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HGVS dbSNP
NM_001035.2(RYR2):c.10231-4T>C rs117180147
NM_001035.2(RYR2):c.10324-4A>G rs72751287
NM_001035.2(RYR2):c.1053A>G (p.Thr351=) rs187565743
NM_001035.2(RYR2):c.1134C>T (p.Asp378=) rs193922621
NM_001035.2(RYR2):c.11557+19C>T rs113408406
NM_001035.2(RYR2):c.1218G>A (p.Ser406=) rs147389346
NM_001035.2(RYR2):c.12492G>A (p.Gln4164=) rs377293019
NM_001035.2(RYR2):c.12648G>A (p.Ala4216=) rs781557399
NM_001035.2(RYR2):c.12705C>T (p.Phe4235=) rs373606009
NM_001035.2(RYR2):c.12858C>T (p.Ser4286=) rs185482345
NM_001035.2(RYR2):c.13260+14A>G rs141528541
NM_001035.2(RYR2):c.13293A>G (p.Glu4431=) rs778248995
NM_001035.2(RYR2):c.13566C>T (p.Val4522=) rs57360419
NM_001035.2(RYR2):c.13977G>A (p.Glu4659=) rs78369334
NM_001035.2(RYR2):c.14029C>T (p.Leu4677=) rs112864477
NM_001035.2(RYR2):c.14091-11dup rs35563566
NM_001035.2(RYR2):c.14101A>G (p.Ile4701Val) rs755065507
NM_001035.2(RYR2):c.14481C>A (p.Ile4827=) rs114303476
NM_001035.2(RYR2):c.14809-15C>G rs790897
NM_001035.2(RYR2):c.1548T>C (p.Asp516=) rs146129084
NM_001035.2(RYR2):c.1611G>A (p.Leu537=) rs78281932
NM_001035.2(RYR2):c.1822C>T (p.His608Tyr) rs727504718
NM_001035.2(RYR2):c.1863C>T (p.His621=) rs17686573
NM_001035.2(RYR2):c.2204-7C>G rs147479514
NM_001035.2(RYR2):c.2301G>T (p.Ser767=) rs117588730
NM_001035.2(RYR2):c.2630A>C (p.His877Pro) rs561321743
NM_001035.2(RYR2):c.3038G>A (p.Arg1013Gln) rs149514924
NM_001035.2(RYR2):c.3599-9delT rs11331089
NM_001035.2(RYR2):c.3849A>G (p.Leu1283=) rs143603583
NM_001035.2(RYR2):c.385-9A>C rs140998248
NM_001035.2(RYR2):c.4734C>T (p.Pro1578=) rs201880756
NM_001035.2(RYR2):c.4989C>T (p.Ala1663=) rs147060179
NM_001035.2(RYR2):c.5001T>C (p.Leu1667=) rs397516537
NM_001035.2(RYR2):c.5586C>T (p.Asp1862=) rs193922628
NM_001035.2(RYR2):c.5654G>A (p.Gly1885Glu) rs41315858
NM_001035.2(RYR2):c.5656G>A (p.Gly1886Ser) rs3766871
NM_001035.2(RYR2):c.684C>T (p.Leu228=) rs72549417
NM_001035.2(RYR2):c.7038A>C (p.Ala2346=) rs116601686
NM_001035.2(RYR2):c.7161G>A (p.Ala2387=) rs371560909
NM_001035.2(RYR2):c.7365C>T (p.Asp2455=) rs72549416
NM_001035.2(RYR2):c.7488C>T (p.Leu2496=) rs143906555
NM_001035.2(RYR2):c.7619A>G (p.His2540Arg) rs200105499
NM_001035.2(RYR2):c.828A>G (p.Arg276=) rs180711819
NM_001035.2(RYR2):c.8873A>G (p.Gln2958Arg) rs34967813
NM_001035.2(RYR2):c.9666C>T (p.Ala3222=) rs116442127
NM_001035.2(RYR2):c.9963G>A (p.Pro3321=) rs199730192

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