ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.993-7G>A

dbSNP: rs2101925873
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001463755 SCV001667702 likely benign Nephronophthisis 2020-07-22 criteria provided, single submitter clinical testing

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