ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.2901C>T (p.Ser967=) (rs570068696)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000532279 SCV000648455 likely benign not provided 2018-02-26 criteria provided, single submitter clinical testing
Ambry Genetics RCV000619751 SCV000735630 likely benign Cardiovascular phenotype 2016-11-25 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV001455931 SCV001659702 likely benign Brugada syndrome 8 2020-11-25 criteria provided, single submitter clinical testing

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