ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.883_885dup (p.Ser295dup)

dbSNP: rs61549495
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244728 SCV000313262 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001513791 SCV001721473 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001513791 SCV001864151 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259746 SCV002539862 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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