ClinVar Miner

List of variants reported as likely pathogenic for Arrhythmogenic right ventricular dysplasia 1; Rienhoff syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.1034C>G (p.Ser345Ter)	rs1060502827
NM_003239.5(TGFB3):c.1102_1105del (p.Leu368fs)	rs1555360047

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