ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.453-11T>C

gnomAD frequency: 0.00004  dbSNP: rs374073392
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002136638 SCV002464029 likely benign not provided 2021-09-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500315 SCV002813605 likely benign Polycystic liver disease 2 2021-12-07 criteria provided, single submitter clinical testing

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