ClinVar Miner

Submissions for variant NC_000001.11:g.156115286C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005099272 SCV005831413 likely benign Charcot-Marie-Tooth disease type 2 2024-07-30 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Wuerzburg RCV003128184 SCV003804382 uncertain significance Cardiomyopathy no assertion criteria provided clinical testing

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