ClinVar Miner

List of variants in gene RYR2 reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 44
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HGVS dbSNP
NM_001035.2(RYR2):c.8437-7dupG rs148246251
NM_001035.3(RYR2):c.10254C>T (p.Asn3418=) rs138073811
NM_001035.3(RYR2):c.10503C>T (p.Thr3501=) rs2797441
NM_001035.3(RYR2):c.10776C>T (p.Ser3592=) rs2685301
NM_001035.3(RYR2):c.10935+18C>T rs2797445
NM_001035.3(RYR2):c.11557+19C>T rs113408406
NM_001035.3(RYR2):c.11963-11T>C rs790889
NM_001035.3(RYR2):c.1218G>A (p.Ser406=) rs147389346
NM_001035.3(RYR2):c.13476+16A>G rs2256242
NM_001035.3(RYR2):c.13564-41A>G rs114289907
NM_001035.3(RYR2):c.1359C>T (p.Ser453=) rs3765097
NM_001035.3(RYR2):c.13740G>A (p.Thr4580=) rs115854664
NM_001035.3(RYR2):c.13783-6A>G rs790901
NM_001035.3(RYR2):c.13913+12A>C rs790900
NM_001035.3(RYR2):c.14029C>T (p.Leu4677=) rs112864477
NM_001035.3(RYR2):c.14481C>A (p.Ile4827=) rs114303476
NM_001035.3(RYR2):c.1612+14T>C rs2045955
NM_001035.3(RYR2):c.1776A>T (p.Gly592=) rs72549414
NM_001035.3(RYR2):c.1863C>T (p.His621=) rs17686573
NM_001035.3(RYR2):c.2301G>T (p.Ser767=) rs117588730
NM_001035.3(RYR2):c.2973A>G (p.Ser991=) rs2253273
NM_001035.3(RYR2):c.3030T>C (p.Asp1010=) rs138064129
NM_001035.3(RYR2):c.3407C>T (p.Ala1136Val) rs72549415
NM_001035.3(RYR2):c.3537T>C (p.Gly1179=) rs397516526
NM_001035.3(RYR2):c.3599-9del rs11331089
NM_001035.3(RYR2):c.3849A>G (p.Leu1283=) rs143603583
NM_001035.3(RYR2):c.464-8A>C rs10925391
NM_001035.3(RYR2):c.4740G>A (p.Pro1580=) rs79811945
NM_001035.3(RYR2):c.5154G>A (p.Arg1718=) rs114534505
NM_001035.3(RYR2):c.5613C>T (p.Asp1871=) rs116774472
NM_001035.3(RYR2):c.5654G>A (p.Gly1885Glu) rs41315858
NM_001035.3(RYR2):c.5656G>A (p.Gly1886Ser) rs3766871
NM_001035.3(RYR2):c.6555+6G>A rs372661934
NM_001035.3(RYR2):c.6555+8C>T rs1759122
NM_001035.3(RYR2):c.677-11T>A rs10754602
NM_001035.3(RYR2):c.6906T>C (p.Leu2302=) rs707189
NM_001035.3(RYR2):c.7038A>C (p.Ala2346=) rs116601686
NM_001035.3(RYR2):c.7365C>T (p.Asp2455=) rs72549416
NM_001035.3(RYR2):c.7488C>T (p.Leu2496=) rs143906555
NM_001035.3(RYR2):c.7806C>T (p.His2602=) rs684923
NM_001035.3(RYR2):c.8448C>T (p.Asp2816=) rs144876996
NM_001035.3(RYR2):c.849-8T>C rs16835237
NM_001035.3(RYR2):c.8873A>G (p.Gln2958Arg) rs34967813
NM_001035.3(RYR2):c.9318T>G (p.Ser3106=) rs2797436

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