ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.3251+31A>G

gnomAD frequency: 0.10053  dbSNP: rs3801304
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001649352 SCV001863033 benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260259 SCV002540029 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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