ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.*3C>T

dbSNP: rs2052197
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001668713 SCV001884872 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260276 SCV002540051 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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