ClinVar Miner

Submissions for variant NM_004924.6(ACTN4):c.2418+28A>G

dbSNP: rs12981131
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650137 SCV001868550 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002253936 SCV002524564 benign Focal segmental glomerulosclerosis 1 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001650137 SCV005310933 benign not provided criteria provided, single submitter not provided

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