ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.10299A>T (p.Thr3433=)

dbSNP: rs2137576092
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001484534 SCV001688953 likely benign Spastic paraplegia 2020-09-02 criteria provided, single submitter clinical testing

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