ClinVar Miner

List of variants in gene RYR1 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 47
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HGVS dbSNP
NM_000540.2(RYR1):c.-108T>C rs4632259
NM_000540.2(RYR1):c.10188C>T (p.Asp3396=) rs2229145
NM_000540.2(RYR1):c.10218C>T (p.Tyr3406=) rs41274330
NM_000540.2(RYR1):c.10687-10C>T rs77592501
NM_000540.2(RYR1):c.10687-7C>T rs2960354
NM_000540.2(RYR1):c.1077T>C (p.Ala359=) rs10406027
NM_000540.2(RYR1):c.11266C>G (p.Gln3756Glu) rs4802584
NM_000540.2(RYR1):c.11754T>A (p.Thr3918=) rs45613041
NM_000540.2(RYR1):c.11908-14A>G rs2292799
NM_000540.2(RYR1):c.12094+11A>G rs73933018
NM_000540.2(RYR1):c.12624+14C>T rs75797287
NM_000540.2(RYR1):c.13671C>G (p.Ser4557=) rs35959206
NM_000540.2(RYR1):c.14256A>C (p.Thr4752=) rs1468571
NM_000540.2(RYR1):c.1668G>A (p.Ser556=) rs2288888
NM_000540.2(RYR1):c.2286C>T (p.Pro762=) rs3745847
NM_000540.2(RYR1):c.2871-5C>T rs45585535
NM_000540.2(RYR1):c.2943G>A (p.Thr981=) rs2228069
NM_000540.2(RYR1):c.2979C>T (p.Asn993=) rs2228070
NM_000540.2(RYR1):c.3456C>T (p.Ile1152=) rs11083462
NM_000540.2(RYR1):c.3858T>C (p.Leu1286=) rs16972636
NM_000540.2(RYR1):c.4024A>G (p.Ser1342Gly) rs34694816
NM_000540.2(RYR1):c.4107C>T (p.Pro1369=) rs11882640
NM_000540.2(RYR1):c.4161-6T>C rs55845760
NM_000540.2(RYR1):c.5112C>T (p.Gly1704=) rs35352076
NM_000540.2(RYR1):c.5334G>T (p.Ser1778=) rs35566549
NM_000540.2(RYR1):c.594A>G (p.Leu198=) rs2229139
NM_000540.2(RYR1):c.6039A>G (p.Lys2013=) rs2228068
NM_000540.2(RYR1):c.6178G>T (p.Gly2060Cys) rs35364374
NM_000540.2(RYR1):c.7089C>T (p.Cys2363=) rs2228071
NM_000540.2(RYR1):c.7098C>T (p.Pro2366=) rs2229147
NM_000540.2(RYR1):c.7209C>T (p.Arg2403=) rs78795178
NM_000540.2(RYR1):c.7260C>T (p.His2420=) rs12973632
NM_000540.2(RYR1):c.7500G>A (p.Ala2500=) rs2228072
NM_000540.2(RYR1):c.7527G>A (p.Val2509=) rs2071088
NM_000540.2(RYR1):c.7614+10C>G rs2960323
NM_000540.2(RYR1):c.7835+5A>G rs1469695
NM_000540.2(RYR1):c.7863C>T (p.His2621=) rs2229142
NM_000540.2(RYR1):c.7872C>T (p.Arg2624=) rs1469698
NM_000540.2(RYR1):c.7977G>A (p.Thr2659=) rs2229144
NM_000540.2(RYR1):c.8118T>C (p.Ile2706=) rs2960340
NM_000540.2(RYR1):c.8190T>C (p.Asp2730=) rs2915951
NM_000540.2(RYR1):c.8337G>A (p.Glu2779=) rs2915952
NM_000540.2(RYR1):c.8589T>C (p.Ser2863=) rs2229146
NM_000540.2(RYR1):c.8693-10G>C rs2915958
NM_000540.2(RYR1):c.9186A>G (p.Pro3062=) rs2071089
NM_000540.2(RYR1):c.9555-13C>T rs2960328
NM_000540.2(RYR1):c.9690G>A (p.Leu3230=) rs2304151

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