ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.999-4A>T

dbSNP: rs910246095
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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 RCV001488295 SCV001692803 likely benign Neuronal ceroid lipofuscinosis 7 2020-08-21 criteria provided, single submitter clinical testing

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