ClinVar Miner

Submissions for variant NM_000521.4(HEXB):c.771+9A>G

dbSNP: rs768648039
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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 RCV001490132 SCV001694690 likely benign Sandhoff disease 2024-02-25 criteria provided, single submitter clinical testing

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