ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.321G>T (p.Gln107His)

dbSNP: rs1554958092
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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 RCV000678927 SCV000805135 likely pathogenic Long QT syndrome 1 2018-01-09 criteria provided, single submitter clinical testing

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