ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.10227A>G (p.Ser3409=)

dbSNP: rs1593123878
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 RCV000902674 SCV001047105 likely benign Spastic paraplegia 2023-09-12 criteria provided, single submitter clinical testing
Natera, Inc. RCV001825815 SCV002086183 likely benign Charlevoix-Saguenay spastic ataxia 2020-04-03 no assertion criteria provided clinical testing

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