ClinVar Miner

Submissions for variant NM_001023570.4(IQCB1):c.393+15A>C

dbSNP: rs369407077
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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 RCV003587739 SCV004315712 likely benign Nephronophthisis 2023-08-17 criteria provided, single submitter clinical testing

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