ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.2937A>G (p.Glu979=)

dbSNP: rs2139746472
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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 RCV001452326 SCV001655984 likely benign Hereditary spastic paraplegia 49 2020-06-07 criteria provided, single submitter clinical testing

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