ClinVar Miner

List of variants in gene RYR2 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 33
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HGVS dbSNP
NM_001035.3(RYR2):c.100A>C (p.Lys34Gln) rs876661385
NM_001035.3(RYR2):c.10125A>G (p.Arg3375=) rs764396074
NM_001035.3(RYR2):c.10231-4T>C rs117180147
NM_001035.3(RYR2):c.10342G>C (p.Glu3448Gln) rs1553298016
NM_001035.3(RYR2):c.10592A>G (p.Tyr3531Cys) rs794728769
NM_001035.3(RYR2):c.1082G>A (p.Cys361Tyr) rs794728719
NM_001035.3(RYR2):c.11218G>T (p.Val3740Leu) rs536555602
NM_001035.3(RYR2):c.11591A>G (p.Asn3864Ser) rs794728776
NM_001035.3(RYR2):c.12056T>C (p.Met4019Thr) rs886039150
NM_001035.3(RYR2):c.13291G>A (p.Glu4431Lys) rs571985775
NM_001035.3(RYR2):c.13520T>C (p.Leu4507Ser) rs794728798
NM_001035.3(RYR2):c.13528G>A (p.Ala4510Thr) rs397516510
NM_001035.3(RYR2):c.13600C>T (p.Pro4534Ser) rs199624074
NM_001035.3(RYR2):c.13763T>C (p.Ile4588Thr) rs876661386
NM_001035.3(RYR2):c.13904T>A (p.Ile4635Asn) rs1060500169
NM_001035.3(RYR2):c.14173T>A (p.Tyr4725Asn) rs876661387
NM_001035.3(RYR2):c.2267G>A (p.Ser756Asn) rs193922623
NM_001035.3(RYR2):c.2828T>C (p.Leu943Ser) rs373665895
NM_001035.3(RYR2):c.3026G>A (p.Arg1009Gln) rs754812132
NM_001035.3(RYR2):c.3251G>A (p.Arg1084Lys) rs193922624
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.3932C>T (p.Ala1311Val) rs757471928
NM_001035.3(RYR2):c.4040T>G (p.Met1347Arg) rs193922625
NM_001035.3(RYR2):c.6445A>G (p.Ile2149Val) rs767258350
NM_001035.3(RYR2):c.649A>G (p.Ile217Val) rs200642525
NM_001035.3(RYR2):c.6757C>G (p.Leu2253Val) rs876661389
NM_001035.3(RYR2):c.8130T>G (p.Asn2710Lys) rs876661388
NM_001035.3(RYR2):c.8145G>T (p.Glu2715Asp) rs200420897
NM_001035.3(RYR2):c.8879T>A (p.Ile2960Asn) rs759048462
NM_001035.3(RYR2):c.9619A>G (p.Asn3207Asp) rs372601642
NM_001035.3(RYR2):c.9655G>A (p.Val3219Met) rs371147744
NM_001035.3(RYR2):c.9887T>C (p.Met3296Thr) rs876661390

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