ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.553A>C (p.Arg185=)

gnomAD frequency: 0.07957  dbSNP: rs61737563
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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 RCV000247760 SCV000313260 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651229 SCV001863719 benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001651229 SCV002414479 benign not provided 2021-03-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259744 SCV002539818 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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