ClinVar Miner

Submissions for variant NM_006070.6(TFG):c.795T>C (p.Pro265=)

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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 RCV005214178 SCV005854376 likely benign Hereditary motor and sensory neuropathy, Okinawa type; Hereditary spastic paraplegia 57 2024-11-30 criteria provided, single submitter clinical testing

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