ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.2778G>T (p.Pro926=)

dbSNP: rs898987242
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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 RCV001396164 SCV001597888 likely benign Long QT syndrome 2016-09-29 criteria provided, single submitter clinical testing

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