ClinVar Miner

Submissions for variant NM_006070.6(TFG):c.594T>G (p.Ala198=) (rs12562)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000525073 SCV000642066 benign Hereditary motor and sensory neuropathy, Okinawa type; Spastic paraplegia 57, autosomal recessive 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001287094 SCV001473740 benign none provided 2020-05-15 criteria provided, single submitter clinical testing

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