ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.1936-27_1936-25dup

dbSNP: rs749125299
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV002496033 SCV002803497 likely benign Polycystic liver disease 2 2021-11-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003688944 SCV004448624 benign not provided 2024-01-12 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702166 SCV001927587 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001702166 SCV001970491 benign not specified no assertion criteria provided clinical testing

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