ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.-185T>C

dbSNP: rs115256710
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001681006 SCV001896106 benign not provided 2020-06-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001681006 SCV005288613 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001827579 SCV002090101 benign Steroid-resistant nephrotic syndrome 2019-10-28 no assertion criteria provided clinical testing

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