ClinVar Miner

List of variants in gene DSG2 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 5
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HGVS dbSNP
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.1945G>A (p.Gly649Ser) rs730880078
NM_001943.5(DSG2):c.2110A>G (p.Ile704Val) rs141388237
NM_001943.5(DSG2):c.2335-7A>G rs528851283
NM_001943.5(DSG2):c.2623A>G (p.Met875Val) rs370316475

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