ClinVar Miner

Submissions for variant NM_016955.4(SEPSECS):c.489G>A (p.Lys163=)

gnomAD frequency: 0.00001  dbSNP: rs587780457
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000118323 SCV000152703 uncertain significance not provided 2013-04-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000118323 SCV002440643 likely benign not provided 2023-06-09 criteria provided, single submitter clinical testing

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