ClinVar Miner

Submissions for variant NM_000520.6(HEXA):c.1147-9_1147-6del

dbSNP: rs2140320865
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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 RCV002164562 SCV002474493 likely benign Tay-Sachs disease 2021-08-25 criteria provided, single submitter clinical testing

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