ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.2181+19G>A

gnomAD frequency: 0.00019  dbSNP: rs201539829
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 RCV002115764 SCV002409878 benign Hereditary spastic paraplegia 7 2023-10-16 criteria provided, single submitter clinical testing
AiLife Diagnostics, AiLife Diagnostics RCV002223340 SCV002501419 uncertain significance not provided 2021-06-02 criteria provided, single submitter clinical testing

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