ClinVar Miner

Submissions for variant NM_007214.5(SEC63):c.340-12del

gnomAD frequency: 0.01010  dbSNP: rs58827902
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000153931 SCV000203548 benign not specified 2013-11-26 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000339022 SCV000459470 benign Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000339022 SCV000459472 benign Polycystic liver disease 1 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV002056047 SCV002404187 benign not provided 2024-01-24 criteria provided, single submitter clinical testing

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