ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.1442-8C>T

dbSNP: rs766872386
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000732298 SCV000860231 uncertain significance not provided 2018-03-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061008 SCV002395806 likely benign Nephronophthisis 2022-07-05 criteria provided, single submitter clinical testing

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