ClinVar Miner

Submissions for variant NM_004409.5(DMPK):c.931C>T (p.Arg311Ter)

dbSNP: rs762280354
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714720 SCV000845447 uncertain significance Steinert myotonic dystrophy syndrome 2021-02-06 criteria provided, single submitter clinical testing

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