ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.2782C>G (p.Pro928Ala)

dbSNP: rs1482640658
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV000853600 SCV000996568 uncertain significance Brugada syndrome 8 2019-04-09 criteria provided, single submitter clinical testing

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