ClinVar Miner

List of variants in gene RYR2 reported as benign by PreventionGenetics

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Total variants: 50
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HGVS dbSNP
NM_001035.2(RYR2):c.8437-7dupG rs148246251
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.11092-25T>C rs3753630
NM_001035.3(RYR2):c.11326-23C>T rs2253831
NM_001035.3(RYR2):c.11557+19C>T rs113408406
NM_001035.3(RYR2):c.11963-11T>C rs790889
NM_001035.3(RYR2):c.1292+20C>T rs182050281
NM_001035.3(RYR2):c.13476+16A>G rs2256242
NM_001035.3(RYR2):c.13476+47G>A rs16835818
NM_001035.3(RYR2):c.13564-41A>G rs114289907
NM_001035.3(RYR2):c.1359C>T (p.Ser453=) rs3765097
NM_001035.3(RYR2):c.13783-21G>A rs790902
NM_001035.3(RYR2):c.13783-6A>G rs790901
NM_001035.3(RYR2):c.13913+12A>C rs790900
NM_001035.3(RYR2):c.14091-25G>A rs9428384
NM_001035.3(RYR2):c.14421C>T (p.Asp4807=) rs75206601
NM_001035.3(RYR2):c.1519G>A (p.Val507Ile) rs16835270
NM_001035.3(RYR2):c.1611G>A (p.Leu537=) rs78281932
NM_001035.3(RYR2):c.1612+14T>C rs2045955
NM_001035.3(RYR2):c.1776A>T (p.Gly592=) rs72549414
NM_001035.3(RYR2):c.1828-49G>T rs66497566
NM_001035.3(RYR2):c.2046A>G (p.Thr682=) rs116098815
NM_001035.3(RYR2):c.2718+26A>G rs2618702
NM_001035.3(RYR2):c.2973A>G (p.Ser991=) rs2253273
NM_001035.3(RYR2):c.3423+49A>G rs2805390
NM_001035.3(RYR2):c.3424-50G>A rs2805396
NM_001035.3(RYR2):c.4160+48A>G rs1332777
NM_001035.3(RYR2):c.4198A>G (p.Ser1400Gly) rs56229512
NM_001035.3(RYR2):c.4275+35C>T rs2618713
NM_001035.3(RYR2):c.4275+50T>C rs2779430
NM_001035.3(RYR2):c.4597-11del rs3841805
NM_001035.3(RYR2):c.464-8A>C rs10925391
NM_001035.3(RYR2):c.4684-11C>T rs7546045
NM_001035.3(RYR2):c.5400A>G (p.Lys1800=) rs3820216
NM_001035.3(RYR2):c.5656G>A (p.Gly1886Ser) rs3766871
NM_001035.3(RYR2):c.576+7G>C rs10925392
NM_001035.3(RYR2):c.6556-28A>G rs12563366
NM_001035.3(RYR2):c.6556-41G>A rs10802626
NM_001035.3(RYR2):c.677-11T>A rs10754602
NM_001035.3(RYR2):c.6906T>C (p.Leu2302=) rs707189
NM_001035.3(RYR2):c.7342+16A>G rs76678214
NM_001035.3(RYR2):c.7806C>T (p.His2602=) rs684923
NM_001035.3(RYR2):c.8209-29A>C rs10925485
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
NM_001035.3(RYR2):c.9449+8T>A rs60777199

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