ClinVar Miner

List of variants in gene RYR2 reported as uncertain significance for Catecholaminergic polymorphic ventricular tachycardia type 1

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Total variants: 18
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HGVS dbSNP
NM_001035.3(RYR2):c.10241G>A (p.Arg3414Lys) rs1131692324
NM_001035.3(RYR2):c.11197G>A (p.Asp3733Asn) rs760307737
NM_001035.3(RYR2):c.11234G>T (p.Ser3745Ile)
NM_001035.3(RYR2):c.1144G>A (p.Val382Met) rs370057029
NM_001035.3(RYR2):c.13291G>A (p.Glu4431Lys) rs571985775
NM_001035.3(RYR2):c.13412G>C (p.Gly4471Ala) rs1553325274
NM_001035.3(RYR2):c.13476+8_13476+11dup rs864309562
NM_001035.3(RYR2):c.1604A>G (p.Glu535Gly) rs869025509
NM_001035.3(RYR2):c.1918A>G (p.Arg640Gly) rs886041109
NM_001035.3(RYR2):c.2306G>T (p.Arg769Leu) rs754901791
NM_001035.3(RYR2):c.2468A>T (p.Tyr823Phe)
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln) rs149514924
NM_001035.3(RYR2):c.4652A>G (p.Asn1551Ser) rs185237690
NM_001035.3(RYR2):c.5585A>G (p.Asp1862Gly) rs1559117209
NM_001035.3(RYR2):c.6394G>C (p.Val2132Leu) rs1553531684
NM_001035.3(RYR2):c.6520G>T (p.Val2174Phe) rs1131692321
NM_001035.3(RYR2):c.7469T>C (p.Val2490Ala) rs886041112
NM_001035.3(RYR2):c.9352G>A (p.Gly3118Arg) rs730880194

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