ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.1506T>C (p.Ser502=)

gnomAD frequency: 0.11596  dbSNP: rs10224902
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513792 SCV001721474 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001513792 SCV001914674 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260156 SCV002539895 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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