ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.2818-2= (rs1217117155)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000153587 SCV000203125 benign not specified 2014-08-26 criteria provided, single submitter clinical testing
Invitae RCV000860026 SCV000999936 benign Nephronophthisis 2019-12-31 criteria provided, single submitter clinical testing
Mendelics RCV000986224 SCV001135156 benign Nephronophthisis 4 2019-05-28 criteria provided, single submitter clinical testing

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