ClinVar Miner

Submissions for variant NC_000011.9:g.(2683312_2790073)_(2799268_2868996)dup

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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 RCV000496727 SCV000588149 likely pathogenic Long QT syndrome 1 2017-03-15 criteria provided, single submitter clinical testing

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