ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.598A>G (p.Ile200Val)

gnomAD frequency: 0.00001  dbSNP: rs762268076
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001067073 SCV001232105 benign Spastic paraplegia 2024-01-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277273 SCV001464191 uncertain significance Charlevoix-Saguenay spastic ataxia 2020-01-17 no assertion criteria provided clinical testing

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