ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.7326A>G (p.Glu2442=)

dbSNP: rs2137601476
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 RCV001461952 SCV001665862 likely benign Spastic paraplegia 2020-11-17 criteria provided, single submitter clinical testing

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