ClinVar Miner

Submissions for variant NM_015161.3(ARL6IP1):c.199C>T (p.Leu67=)

gnomAD frequency: 0.00006  dbSNP: rs763110010
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 RCV001520143 SCV001729181 benign Hereditary spastic paraplegia 61 2025-01-22 criteria provided, single submitter clinical testing

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