ClinVar Miner

Submissions for variant NM_001776.6(ENTPD1):c.16+13T>C

dbSNP: rs766973012
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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 RCV002098912 SCV002434512 likely benign Hereditary spastic paraplegia 64 2024-12-03 criteria provided, single submitter clinical testing

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