ClinVar Miner

Submissions for variant NM_000520.6(HEXA):c.1074-12TCTCC[3]

dbSNP: rs759219683
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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 RCV002150223 SCV002418499 likely benign Tay-Sachs disease 2024-05-20 criteria provided, single submitter clinical testing

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