ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.1493_1494inv (p.Asn498Ser)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001521352 SCV001730681 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501836 SCV002805681 likely benign Retinitis pigmentosa 38 2021-10-22 criteria provided, single submitter clinical testing

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