ClinVar Miner

Submissions for variant NM_006070.6(TFG):c.288C>G (p.Pro96=)

dbSNP: rs1180461235
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001455916 SCV001659686 likely benign Hereditary motor and sensory neuropathy, Okinawa type; Hereditary spastic paraplegia 57 2024-09-02 criteria provided, single submitter clinical testing

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