ClinVar Miner

Submissions for variant NM_003661.4(APOL1):c.390C>T (p.His130=)

gnomAD frequency: 0.00005  dbSNP: rs760970273
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002148288 SCV002461000 likely benign not provided 2021-10-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494456 SCV002800402 likely benign Focal segmental glomerulosclerosis 4, susceptibility to 2021-11-04 criteria provided, single submitter clinical testing

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