ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.275-2A>G

dbSNP: rs1553315173
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673930 SCV000799187 likely pathogenic Nephrotic syndrome, type 2 2018-04-11 criteria provided, single submitter clinical testing
Baylor Genetics RCV000673930 SCV005053675 likely pathogenic Nephrotic syndrome, type 2 2024-03-26 criteria provided, single submitter clinical testing

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