ClinVar Miner

Submissions for variant NM_022098.4(XPNPEP3):c.774T>C (p.Ala258=)

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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 RCV002766034 SCV003022359 likely benign Nephronophthisis-like nephropathy 1 2024-01-17 criteria provided, single submitter clinical testing

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