ClinVar Miner

Submissions for variant NM_017636.4(TRPM4):c.1496G>A (p.Arg499Gln)

dbSNP: rs2122936347
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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 RCV001541906 SCV001760550 uncertain significance Cardiomyopathy no assertion criteria provided clinical testing

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