ClinVar Miner

Submissions for variant NM_018400.3(SCN3B):c.438C>T (p.Thr146=) (rs1275085)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244052 SCV000313225 benign not specified criteria provided, single submitter clinical testing
Ambry Genetics RCV000241560 SCV000318133 benign Cardiovascular phenotype 2015-06-23 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000339303 SCV000368399 likely benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000860457 SCV001000516 benign not provided 2019-03-06 criteria provided, single submitter clinical testing

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