ClinVar Miner

Submissions for variant NM_001776.6(ENTPD1):c.858A>G (p.Gly286=)

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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 RCV002626341 SCV002966214 likely benign Hereditary spastic paraplegia 64 2024-06-26 criteria provided, single submitter clinical testing

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