ClinVar Miner

Submissions for variant NM_001353214.3(DYM):c.2172C>T (p.Asp724=)

gnomAD frequency: 0.00052  dbSNP: rs201928717
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000597311 SCV000709454 likely benign not specified 2017-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000886145 SCV001029633 benign not provided 2022-12-22 criteria provided, single submitter clinical testing

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