ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.126G>A (p.Gly42=)

gnomAD frequency: 0.00007  dbSNP: rs769791509
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000900255 SCV001044562 likely benign not provided 2023-12-14 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276839 SCV001463422 likely benign Steroid-resistant nephrotic syndrome 2020-06-18 no assertion criteria provided clinical testing

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