ClinVar Miner

List of variants in gene RYR2 reported as uncertain significance by Color

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Total variants: 93
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HGVS dbSNP
NM_001035.3(RYR2):c.10096C>T (p.Leu3366Phe) rs377712921
NM_001035.3(RYR2):c.10373G>A (p.Arg3458Gln) rs762944627
NM_001035.3(RYR2):c.10662A>G (p.Ile3554Met) rs1558290857
NM_001035.3(RYR2):c.10975A>G (p.Lys3659Glu) rs184527312
NM_001035.3(RYR2):c.11002A>G (p.Ile3668Val) rs1558307580
NM_001035.3(RYR2):c.1144G>A (p.Val382Met) rs370057029
NM_001035.3(RYR2):c.11497G>A (p.Asp3833Asn) rs768711283
NM_001035.3(RYR2):c.11552A>G (p.Asn3851Ser) rs967116157
NM_001035.3(RYR2):c.12091A>G (p.Thr4031Ala) rs755148895
NM_001035.3(RYR2):c.12092C>A (p.Thr4031Asn) rs781478740
NM_001035.3(RYR2):c.12171C>G (p.His4057Gln) rs1558404274
NM_001035.3(RYR2):c.12215C>T (p.Thr4072Met) rs928224285
NM_001035.3(RYR2):c.12331A>C (p.Asn4111His) rs192890834
NM_001035.3(RYR2):c.1243A>G (p.Thr415Ala) rs545357663
NM_001035.3(RYR2):c.12700G>A (p.Ala4234Thr) rs773317989
NM_001035.3(RYR2):c.12778A>G (p.Ser4260Gly) rs1416980159
NM_001035.3(RYR2):c.12859T>C (p.Tyr4287His) rs190009333
NM_001035.3(RYR2):c.12919C>T (p.Arg4307Cys) rs200092869
NM_001035.3(RYR2):c.13130C>T (p.Ser4377Leu) rs869025514
NM_001035.3(RYR2):c.13213C>T (p.Leu4405Phe)
NM_001035.3(RYR2):c.13220G>A (p.Ser4407Asn) rs755585430
NM_001035.3(RYR2):c.13291G>A (p.Glu4431Lys) rs571985775
NM_001035.3(RYR2):c.1345A>G (p.Ile449Val) rs775428443
NM_001035.3(RYR2):c.137T>C (p.Leu46Pro) rs931490334
NM_001035.3(RYR2):c.13903A>G (p.Ile4635Val) rs1558429505
NM_001035.3(RYR2):c.1454G>A (p.Arg485Gln) rs752144775
NM_001035.3(RYR2):c.1476+4C>T rs369442980
NM_001035.3(RYR2):c.14818G>A (p.Val4940Ile) rs1558506940
NM_001035.3(RYR2):c.1939C>T (p.Arg647Cys) rs202040519
NM_001035.3(RYR2):c.2045C>G (p.Thr682Arg) rs377285489
NM_001035.3(RYR2):c.2104G>A (p.Gly702Arg) rs569386030
NM_001035.3(RYR2):c.2449C>G (p.Pro817Ala) rs780266883
NM_001035.3(RYR2):c.2450C>T (p.Pro817Leu) rs747582933
NM_001035.3(RYR2):c.2573C>T (p.Thr858Met) rs377068202
NM_001035.3(RYR2):c.2635G>C (p.Glu879Gln) rs576214225
NM_001035.3(RYR2):c.2717C>T (p.Pro906Leu) rs397516522
NM_001035.3(RYR2):c.284T>A (p.Val95Glu) rs900519025
NM_001035.3(RYR2):c.2881G>A (p.Val961Met) rs876657990
NM_001035.3(RYR2):c.2890A>C (p.Met964Leu) rs1362839960
NM_001035.3(RYR2):c.2943G>T (p.Met981Ile) rs1559007743
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln) rs149514924
NM_001035.3(RYR2):c.3122G>A (p.Arg1041Gln) rs773781713
NM_001035.3(RYR2):c.3199C>G (p.Pro1067Ala) rs778889621
NM_001035.3(RYR2):c.3220A>G (p.Arg1074Gly) rs1559038380
NM_001035.3(RYR2):c.3226G>A (p.Glu1076Lys) rs781547572
NM_001035.3(RYR2):c.3266G>A (p.Arg1089His) rs552564367
NM_001035.3(RYR2):c.3320C>T (p.Thr1107Met) rs200236750
NM_001035.3(RYR2):c.3356G>A (p.Arg1119His) rs201312753
NM_001035.3(RYR2):c.3425C>T (p.Ala1142Val) rs772148152
NM_001035.3(RYR2):c.3484G>A (p.Val1162Met) rs377030538
NM_001035.3(RYR2):c.36G>C (p.Gln12His) rs746811389
NM_001035.3(RYR2):c.3721G>A (p.Val1241Ile) rs185715460
NM_001035.3(RYR2):c.3845G>A (p.Cys1282Tyr) rs1559075923
NM_001035.3(RYR2):c.3875C>G (p.Ser1292Cys) rs1559075982
NM_001035.3(RYR2):c.3883A>G (p.Ser1295Gly) rs200574919
NM_001035.3(RYR2):c.4076T>C (p.Val1359Ala) rs1005458283
NM_001035.3(RYR2):c.4384G>A (p.Val1462Ile) rs755547916
NM_001035.3(RYR2):c.4465T>C (p.Cys1489Arg) rs200450676
NM_001035.3(RYR2):c.4780G>A (p.Val1594Ile) rs794728737
NM_001035.3(RYR2):c.4802A>G (p.Asn1601Ser) rs1474971861
NM_001035.3(RYR2):c.4831A>G (p.Ile1611Val) rs755572625
NM_001035.3(RYR2):c.5011C>T (p.Arg1671Trp) rs747404408
NM_001035.3(RYR2):c.5021A>G (p.His1674Arg) rs771414167
NM_001035.3(RYR2):c.5593G>A (p.Glu1865Lys) rs553819263
NM_001035.3(RYR2):c.5617G>A (p.Ala1873Thr) rs1312516879
NM_001035.3(RYR2):c.6203G>A (p.Arg2068Gln)
NM_001035.3(RYR2):c.6307C>G (p.Pro2103Ala) rs1559136427
NM_001035.3(RYR2):c.6332T>C (p.Val2111Ala) rs548415985
NM_001035.3(RYR2):c.6337G>A (p.Val2113Met) rs186906598
NM_001035.3(RYR2):c.6433G>C (p.Gly2145Arg) rs587782974
NM_001035.3(RYR2):c.6677G>A (p.Ser2226Asn) rs1558104099
NM_001035.3(RYR2):c.6799C>T (p.Arg2267Cys) rs554220274
NM_001035.3(RYR2):c.6952A>G (p.Asn2318Asp) rs1006334960
NM_001035.3(RYR2):c.7102T>G (p.Ser2368Ala) rs1558117178
NM_001035.3(RYR2):c.723G>A (p.Met241Ile) rs1558733902
NM_001035.3(RYR2):c.7303G>T (p.Val2435Phe) rs188835713
NM_001035.3(RYR2):c.815G>T (p.Arg272Leu) rs377368967
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr) rs201500134
NM_001035.3(RYR2):c.8218G>A (p.Gly2740Arg) rs1558161320
NM_001035.3(RYR2):c.8240A>T (p.Tyr2747Phe) rs1558161375
NM_001035.3(RYR2):c.8414G>A (p.Arg2805His) rs1247067433
NM_001035.3(RYR2):c.8449G>A (p.Ala2817Thr) rs527576067
NM_001035.3(RYR2):c.8591G>A (p.Gly2864Glu) rs1186402933
NM_001035.3(RYR2):c.8791C>T (p.Arg2931Cys) rs777983238
NM_001035.3(RYR2):c.8816_8817AT[1] (p.Ile2940fs)
NM_001035.3(RYR2):c.8899G>A (p.Val2967Ile) rs751546090
NM_001035.3(RYR2):c.8927A>G (p.Lys2976Arg) rs1558206523
NM_001035.3(RYR2):c.9190G>A (p.Ala3064Thr) rs375482798
NM_001035.3(RYR2):c.9410T>C (p.Leu3137Ser) rs1558249705
NM_001035.3(RYR2):c.9442G>A (p.Val3148Met) rs876657994
NM_001035.3(RYR2):c.9518C>T (p.Thr3173Ile) rs746161154
NM_001035.3(RYR2):c.9569G>A (p.Arg3190Gln) rs369276868
NM_001035.3(RYR2):c.9619A>G (p.Asn3207Asp) rs372601642

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