ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.3876G>A (p.Val1292=)

dbSNP: rs2139803008
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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 RCV002157893 SCV002426829 likely benign Hereditary spastic paraplegia 49 2021-10-18 criteria provided, single submitter clinical testing

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