ClinVar Miner

Submissions for variant NM_004621.6(TRPC6):c.523C>T (p.Arg175Trp) (rs869025541)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000208455 SCV000264268 uncertain significance Nephrotic syndrome 2015-01-19 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000713890 SCV000844530 uncertain significance not provided 2018-07-31 criteria provided, single submitter clinical testing

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