ClinVar Miner

List of variants in gene RYR2 reported as uncertain significance by CSER_CC_NCGL; University of Washington Medical Center

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Total variants: 11
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HGVS dbSNP
NM_001035.3(RYR2):c.11968G>A (p.Val3990Ile) rs1210103464
NM_001035.3(RYR2):c.12023A>G (p.Asn4008Ser) rs1330847491
NM_001035.3(RYR2):c.13666G>A (p.Ala4556Thr) rs189345192
NM_001035.3(RYR2):c.1396C>G (p.Pro466Ala) rs376612295
NM_001035.3(RYR2):c.2402G>T (p.Arg801Leu) rs371157868
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln) rs149514924
NM_001035.3(RYR2):c.3484G>A (p.Val1162Met) rs377030538
NM_001035.3(RYR2):c.4196C>A (p.Thr1399Lys) rs75901196
NM_001035.3(RYR2):c.556G>A (p.Val186Met) rs201211033
NM_001035.3(RYR2):c.5822G>A (p.Arg1941His) rs373600053
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr) rs201500134

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