ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.798G>A (p.Gln266=)

dbSNP: rs2148882297
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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 RCV002161444 SCV002477230 likely benign Neuronal ceroid lipofuscinosis 7 2021-05-05 criteria provided, single submitter clinical testing

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