ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.951+39T>C

gnomAD frequency: 0.03312  dbSNP: rs74384941
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000248991 SCV000309708 likely benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000248991 SCV000700408 benign not specified 2017-02-09 criteria provided, single submitter clinical testing
GeneDx RCV001675723 SCV001893668 benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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