ClinVar Miner

Submissions for variant NM_015271.5(TRIM2):c.1918G>T (p.Gly640Cys)

dbSNP: rs1579721449
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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, University of Wuerzburg RCV000850295 SCV000992470 uncertain significance Peripheral axonal neuropathy no assertion criteria provided clinical testing

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