ClinVar Miner

Submissions for variant NM_007288.3(MME):c.769C>A (p.Arg257Ser) (rs145687755)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics,Cologne University RCV000664251 SCV000787819 uncertain significance Autosomal recessive axonal hereditary motor and sensory neuropathy 2018-04-26 no assertion criteria provided clinical testing

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