ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.874-56A>G

gnomAD frequency: 0.13844  dbSNP: rs10227127
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001646031 SCV001860134 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260251 SCV002539851 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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