ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.873T>A (p.Thr291=)

dbSNP: rs1737992977
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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 RCV001479207 SCV001683500 likely benign Neuronal ceroid lipofuscinosis 7 2023-07-14 criteria provided, single submitter clinical testing

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