ClinVar Miner

Submissions for variant NM_006070.6(TFG):c.552G>C (p.Ala184=)

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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 RCV002750978 SCV003020911 likely benign Hereditary motor and sensory neuropathy, Okinawa type; Hereditary spastic paraplegia 57 2022-06-06 criteria provided, single submitter clinical testing

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