ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.554G>A (p.Arg185Lys)

gnomAD frequency: 0.58104  dbSNP: rs197367
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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 RCV000252709 SCV000313261 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001518340 SCV001727013 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001518340 SCV001940414 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259745 SCV002539829 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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