ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.615C>T (p.Ser205=)

gnomAD frequency: 0.00001  dbSNP: rs778514784
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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 RCV000925910 SCV001071465 likely benign not provided 2024-02-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276837 SCV001463420 uncertain significance Steroid-resistant nephrotic syndrome 2020-05-01 no assertion criteria provided clinical testing

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