ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.655G>A (p.Asp219Asn)

dbSNP: rs1584865954
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000821468 SCV000962225 uncertain significance Long QT syndrome 2021-08-27 criteria provided, single submitter clinical testing

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