ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.7785A>G (p.Pro2595=)

dbSNP: rs2137597409
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 RCV002079535 SCV002429749 likely benign Spastic paraplegia 2022-06-27 criteria provided, single submitter clinical testing

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