ClinVar Miner

List of variants in gene RYR2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 104
Download table as spreadsheet
HGVS dbSNP
NM_001035.2(RYR2):c.8437-7dupG rs148246251
NM_001035.3(RYR2):c.*1108A>G rs540171235
NM_001035.3(RYR2):c.*1160A>G rs114925843
NM_001035.3(RYR2):c.*130G>A rs12725752
NM_001035.3(RYR2):c.*218T>G
NM_001035.3(RYR2):c.*399A>G
NM_001035.3(RYR2):c.*55T>C
NM_001035.3(RYR2):c.*646del rs377407067
NM_001035.3(RYR2):c.*647C>T rs16835894
NM_001035.3(RYR2):c.*787C>A rs143228973
NM_001035.3(RYR2):c.*890_*893dup rs10667874
NM_001035.3(RYR2):c.*980T>C
NM_001035.3(RYR2):c.10017C>T (p.His3339=) rs376439588
NM_001035.3(RYR2):c.1006-12C>T rs367998175
NM_001035.3(RYR2):c.10231-4T>C rs117180147
NM_001035.3(RYR2):c.10231-5C>T rs186326951
NM_001035.3(RYR2):c.10254C>T (p.Asn3418=) rs138073811
NM_001035.3(RYR2):c.10324-4A>G rs72751287
NM_001035.3(RYR2):c.10517G>A (p.Arg3506Gln) rs748805290
NM_001035.3(RYR2):c.1053A>G (p.Thr351=) rs187565743
NM_001035.3(RYR2):c.10962A>C (p.Glu3654Asp) rs547005691
NM_001035.3(RYR2):c.11092-10A>T rs577119352
NM_001035.3(RYR2):c.11476+15C>T rs192323827
NM_001035.3(RYR2):c.11557+14C>T rs374155447
NM_001035.3(RYR2):c.11835C>T (p.Val3945=) rs78939657
NM_001035.3(RYR2):c.11880+13_11880+16del rs199562036
NM_001035.3(RYR2):c.11988C>T (p.Gly3996=) rs56226196
NM_001035.3(RYR2):c.12159G>A (p.Glu4053=) rs41267517
NM_001035.3(RYR2):c.1218G>A (p.Ser406=) rs147389346
NM_001035.3(RYR2):c.12315C>T (p.Leu4105=) rs184625125
NM_001035.3(RYR2):c.12627G>A (p.Ser4209=) rs3753631
NM_001035.3(RYR2):c.12858C>T (p.Ser4286=) rs185482345
NM_001035.3(RYR2):c.12919C>T (p.Arg4307Cys) rs200092869
NM_001035.3(RYR2):c.13137C>A (p.Ile4379=) rs369917806
NM_001035.3(RYR2):c.13220G>A (p.Ser4407Asn) rs755585430
NM_001035.3(RYR2):c.13260+14A>G rs141528541
NM_001035.3(RYR2):c.13291G>A (p.Glu4431Lys) rs571985775
NM_001035.3(RYR2):c.13656T>C (p.His4552=) rs397516512
NM_001035.3(RYR2):c.13740G>A (p.Thr4580=) rs115854664
NM_001035.3(RYR2):c.13977G>A (p.Glu4659=) rs78369334
NM_001035.3(RYR2):c.13983C>T (p.Tyr4661=) rs138498780
NM_001035.3(RYR2):c.14029C>T (p.Leu4677=) rs112864477
NM_001035.3(RYR2):c.14220C>T (p.Ala4740=) rs368971586
NM_001035.3(RYR2):c.14299-12A>G rs41267519
NM_001035.3(RYR2):c.14481C>A (p.Ile4827=) rs114303476
NM_001035.3(RYR2):c.14481C>T (p.Ile4827=) rs114303476
NM_001035.3(RYR2):c.14756+12C>T rs2275693
NM_001035.3(RYR2):c.14809-15C>G rs790897
NM_001035.3(RYR2):c.1519G>A (p.Val507Ile) rs16835270
NM_001035.3(RYR2):c.1548T>C (p.Asp516=) rs146129084
NM_001035.3(RYR2):c.1789A>G (p.Ile597Val)
NM_001035.3(RYR2):c.1863C>T (p.His621=) rs17686573
NM_001035.3(RYR2):c.2046A>G (p.Thr682=) rs116098815
NM_001035.3(RYR2):c.2204-7C>G rs147479514
NM_001035.3(RYR2):c.2267G>A (p.Ser756Asn) rs193922623
NM_001035.3(RYR2):c.2301G>T (p.Ser767=) rs117588730
NM_001035.3(RYR2):c.2574G>A (p.Thr858=) rs367992907
NM_001035.3(RYR2):c.2643A>C (p.Ile881=) rs751869107
NM_001035.3(RYR2):c.2760G>A (p.Glu920=) rs186181155
NM_001035.3(RYR2):c.2910C>T (p.Tyr970=) rs575899061
NM_001035.3(RYR2):c.3030T>C (p.Asp1010=) rs138064129
NM_001035.3(RYR2):c.3054T>C (p.Tyr1018=) rs113422365
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.3598+13T>C
NM_001035.3(RYR2):c.3729A>C (p.Thr1243=) rs536080941
NM_001035.3(RYR2):c.3766C>A (p.Pro1256Thr)
NM_001035.3(RYR2):c.4068C>T (p.Pro1356=) rs199821105
NM_001035.3(RYR2):c.4094C>T (p.Ala1365Val) rs373261115
NM_001035.3(RYR2):c.4198A>G (p.Ser1400Gly) rs56229512
NM_001035.3(RYR2):c.4445G>A (p.Arg1482His) rs373024059
NM_001035.3(RYR2):c.4597-11del rs3841805
NM_001035.3(RYR2):c.4605G>A (p.Pro1535=) rs201916326
NM_001035.3(RYR2):c.463+14G>A
NM_001035.3(RYR2):c.4695T>C (p.Pro1565=) rs368826662
NM_001035.3(RYR2):c.4734C>T (p.Pro1578=) rs201880756
NM_001035.3(RYR2):c.4989C>T (p.Ala1663=) rs147060179
NM_001035.3(RYR2):c.5154G>A (p.Arg1718=) rs114534505
NM_001035.3(RYR2):c.5294C>G (p.Ser1765Cys) rs564806219
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.5656G>A (p.Gly1886Ser) rs3766871
NM_001035.3(RYR2):c.576+7G>C rs10925392
NM_001035.3(RYR2):c.577-14G>A rs148019277
NM_001035.3(RYR2):c.6337G>A (p.Val2113Met) rs186906598
NM_001035.3(RYR2):c.649A>G (p.Ile217Val) rs200642525
NM_001035.3(RYR2):c.6555+6G>A rs372661934
NM_001035.3(RYR2):c.6555+8C>T rs1759122
NM_001035.3(RYR2):c.6689-12T>C rs370972311
NM_001035.3(RYR2):c.684C>T (p.Leu228=) rs72549417
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.7542G>A (p.Leu2514=) rs371088367
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr) rs201500134
NM_001035.3(RYR2):c.8515-7A>G rs766622060
NM_001035.3(RYR2):c.8873A>G (p.Gln2958Arg) rs34967813
NM_001035.3(RYR2):c.9601G>A (p.Val3201Met) rs762549821
NM_001035.3(RYR2):c.9655G>A (p.Val3219Met) rs371147744
NM_001035.3(RYR2):c.9666C>T (p.Ala3222=) rs116442127
NM_001035.3(RYR2):c.9867G>A (p.Gly3289=) rs190537182
NM_001035.3(RYR2):c.9927A>G (p.Lys3309=) rs184937795
NM_001035.3(RYR2):c.9963G>A (p.Pro3321=) rs199730192
NM_001035.3(RYR2):c.9995C>T (p.Thr3332Met) rs774437805

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.