ClinVar Miner

Submissions for variant NM_001776.6(ENTPD1):c.574-20G>A

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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 RCV002903170 SCV003247833 likely benign Hereditary spastic paraplegia 64 2022-04-04 criteria provided, single submitter clinical testing

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