ClinVar Miner

Submissions for variant NM_000521.4(HEXB):c.772-8T>C

dbSNP: rs540508015
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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 RCV002153217 SCV002460359 likely benign Sandhoff disease 2021-07-08 criteria provided, single submitter clinical testing

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