ClinVar Miner

List of variants in gene RYR3 reported as uncertain significance for Inborn genetic diseases

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Total variants: 4
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HGVS dbSNP
NM_001036.5(RYR3):c.11351T>C (p.Phe3784Ser) rs1555480351
NM_001036.5(RYR3):c.8569A>G (p.Lys2857Glu) rs869312926
NM_001036.5(RYR3):c.9290T>G (p.Val3097Gly) rs1555456665
NM_001036.5(RYR3):c.9799C>T (p.Pro3267Ser) rs182972491

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