ClinVar Miner

List of variants in gene RYR2 reported as likely benign for Cardiovascular phenotype

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Total variants: 85
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HGVS dbSNP
NM_001035.3(RYR2):c.10017C>T (p.His3339=) rs376439588
NM_001035.3(RYR2):c.10035G>A (p.Arg3345=) rs754976419
NM_001035.3(RYR2):c.10200T>C (p.Ala3400=) rs779316628
NM_001035.3(RYR2):c.10227C>G (p.Ser3409=) rs1553294531
NM_001035.3(RYR2):c.10254C>T (p.Asn3418=) rs138073811
NM_001035.3(RYR2):c.10324-4A>G rs72751287
NM_001035.3(RYR2):c.10941T>G (p.Pro3647=) rs370332882
NM_001035.3(RYR2):c.11208G>C (p.Ala3736=) rs750384592
NM_001035.3(RYR2):c.1134C>T (p.Asp378=) rs193922621
NM_001035.3(RYR2):c.1135G>A (p.Val379Met) rs199693714
NM_001035.3(RYR2):c.1143C>T (p.Ser381=) rs368844286
NM_001035.3(RYR2):c.11766G>A (p.Glu3922=) rs774625105
NM_001035.3(RYR2):c.12114T>C (p.Asp4038=) rs368103385
NM_001035.3(RYR2):c.12159G>A (p.Glu4053=) rs41267517
NM_001035.3(RYR2):c.12492G>A (p.Gln4164=) rs377293019
NM_001035.3(RYR2):c.12627G>A (p.Ser4209=) rs3753631
NM_001035.3(RYR2):c.12648G>A (p.Ala4216=) rs781557399
NM_001035.3(RYR2):c.12705C>T (p.Phe4235=) rs373606009
NM_001035.3(RYR2):c.1296C>A (p.Gly432=) rs184176405
NM_001035.3(RYR2):c.13137C>A (p.Ile4379=) rs369917806
NM_001035.3(RYR2):c.13326C>T (p.Ala4442=) rs768161152
NM_001035.3(RYR2):c.13635A>T (p.Thr4545=) rs779762647
NM_001035.3(RYR2):c.13656T>C (p.His4552=) rs397516512
NM_001035.3(RYR2):c.13689G>A (p.Glu4563=) rs886039157
NM_001035.3(RYR2):c.13974A>G (p.Gly4658=) rs374606415
NM_001035.3(RYR2):c.13983C>T (p.Tyr4661=) rs138498780
NM_001035.3(RYR2):c.14013C>A (p.Gly4671=) rs1416459319
NM_001035.3(RYR2):c.14079C>G (p.Ser4693=) rs1553330741
NM_001035.3(RYR2):c.14220C>T (p.Ala4740=) rs368971586
NM_001035.3(RYR2):c.14484G>T (p.Gly4828=) rs370996795
NM_001035.3(RYR2):c.14493C>T (p.Ile4831=) rs375456172
NM_001035.3(RYR2):c.14703G>C (p.Val4901=) rs201371633
NM_001035.3(RYR2):c.1527C>T (p.Ser509=) rs886042568
NM_001035.3(RYR2):c.1548T>C (p.Asp516=) rs146129084
NM_001035.3(RYR2):c.1614G>A (p.Ala538=) rs566885717
NM_001035.3(RYR2):c.1665C>T (p.Leu555=) rs371262363
NM_001035.3(RYR2):c.198C>G (p.Thr66=) rs1182284048
NM_001035.3(RYR2):c.2454G>A (p.Gly818=) rs769137517
NM_001035.3(RYR2):c.2574G>A (p.Thr858=) rs367992907
NM_001035.3(RYR2):c.2760G>A (p.Glu920=) rs186181155
NM_001035.3(RYR2):c.2772G>A (p.Leu924=) rs780664060
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln) rs149514924
NM_001035.3(RYR2):c.3054T>C (p.Tyr1018=) rs113422365
NM_001035.3(RYR2):c.3153C>T (p.Arg1051=) rs397516524
NM_001035.3(RYR2):c.3251G>A (p.Arg1084Lys) rs193922624
NM_001035.3(RYR2):c.3294C>T (p.Ala1098=) rs773622667
NM_001035.3(RYR2):c.3372G>A (p.Pro1124=) rs368017980
NM_001035.3(RYR2):c.3720C>T (p.Ala1240=) rs750335699
NM_001035.3(RYR2):c.3834C>T (p.Asp1278=) rs1553514916
NM_001035.3(RYR2):c.3888C>T (p.Asn1296=) rs373721253
NM_001035.3(RYR2):c.3910C>T (p.Leu1304=) rs555317545
NM_001035.3(RYR2):c.4044G>A (p.Lys1348=) rs755391572
NM_001035.3(RYR2):c.4347T>C (p.Asp1449=) rs368930040
NM_001035.3(RYR2):c.4652A>G (p.Asn1551Ser) rs185237690
NM_001035.3(RYR2):c.4695T>C (p.Pro1565=) rs368826662
NM_001035.3(RYR2):c.4761C>T (p.His1587=) rs369612535
NM_001035.3(RYR2):c.4902G>A (p.Glu1634=) rs767794262
NM_001035.3(RYR2):c.5001T>C (p.Leu1667=) rs397516537
NM_001035.3(RYR2):c.5136C>T (p.Ser1712=) rs397516540
NM_001035.3(RYR2):c.5199G>A (p.Thr1733=) rs758505260
NM_001035.3(RYR2):c.5253C>T (p.Ile1751=) rs745565940
NM_001035.3(RYR2):c.5487G>T (p.Leu1829=) rs371250741
NM_001035.3(RYR2):c.5571G>A (p.Pro1857=) rs371934582
NM_001035.3(RYR2):c.5586C>T (p.Asp1862=) rs193922628
NM_001035.3(RYR2):c.5619A>G (p.Ala1873=) rs373282364
NM_001035.3(RYR2):c.5637T>C (p.Gly1879=) rs751554639
NM_001035.3(RYR2):c.6337G>A (p.Val2113Met) rs186906598
NM_001035.3(RYR2):c.6780G>A (p.Pro2260=) rs758855412
NM_001035.3(RYR2):c.7161G>A (p.Ala2387=) rs371560909
NM_001035.3(RYR2):c.7233C>T (p.Ala2411=) rs367994477
NM_001035.3(RYR2):c.726C>T (p.Asp242=) rs76380341
NM_001035.3(RYR2):c.7314C>T (p.Ile2438=) rs374418643
NM_001035.3(RYR2):c.7365C>T (p.Asp2455=) rs72549416
NM_001035.3(RYR2):c.7443A>G (p.Gln2481=) rs759314800
NM_001035.3(RYR2):c.7542G>A (p.Leu2514=) rs371088367
NM_001035.3(RYR2):c.8028G>A (p.Leu2676=) rs775159757
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr) rs201500134
NM_001035.3(RYR2):c.828A>G (p.Arg276=) rs180711819
NM_001035.3(RYR2):c.8367T>C (p.Ile2789=) rs563219502
NM_001035.3(RYR2):c.8631G>A (p.Leu2877=) rs1060503848
NM_001035.3(RYR2):c.9519T>C (p.Thr3173=) rs371931287
NM_001035.3(RYR2):c.9560A>G (p.Lys3187Arg) rs184218219
NM_001035.3(RYR2):c.9672C>T (p.Ser3224=) rs370740528
NM_001035.3(RYR2):c.9942C>G (p.Leu3314=) rs746973997
NM_001035.3(RYR2):c.9996G>A (p.Thr3332=) rs760131228

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