ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.340-8_340-7del

dbSNP: rs66526324
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000293220 SCV000459465 uncertain significance Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001850877 SCV002244271 likely benign not provided 2023-11-10 criteria provided, single submitter clinical testing

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