ClinVar Miner

List of variants reported as likely benign for arrhythmogenic right ventricular dysplasia 13 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (1):

Arrhythmogenic right ventricular dysplasia 13

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.779A>G (p.Gln260Arg)	rs190073606	0.00022

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