ClinVar Miner

Submissions for variant NM_001289104.2(PRKCSH):c.1461+23A>T

dbSNP: rs146086973
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001561123 SCV001783661 likely benign not provided 2018-10-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001561123 SCV005209476 likely benign not provided criteria provided, single submitter not provided

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