ClinVar Miner

Submissions for variant NM_018685.5(ANLN):c.2300-37G>A

gnomAD frequency: 0.22848  dbSNP: rs2302526
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001641657 SCV001855900 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260242 SCV002539962 benign Focal segmental glomerulosclerosis 8 2021-12-05 criteria provided, single submitter clinical testing

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