ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.1206G>T (p.Ser402=)

dbSNP: rs772377066
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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 RCV001409711 SCV001611743 likely benign Neuronal ceroid lipofuscinosis 7 2023-05-22 criteria provided, single submitter clinical testing

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