ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.125-13del

dbSNP: rs565329945
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000309923 SCV000459477 likely benign Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502368 SCV002805513 likely benign Polycystic liver disease 2 2021-09-27 criteria provided, single submitter clinical testing
Invitae RCV003766041 SCV004614694 likely benign not provided 2023-10-22 criteria provided, single submitter clinical testing

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