ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.87C>T (p.Ala29=)

dbSNP: rs12123397
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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 RCV001498669 SCV001703422 likely benign not provided 2023-12-14 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826339 SCV002090098 likely benign Steroid-resistant nephrotic syndrome 2021-10-14 no assertion criteria provided clinical testing

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