ClinVar Miner

Submissions for variant NM_001353214.3(DYM):c.1126-72A>T

gnomAD frequency: 0.01903  dbSNP: rs116154576
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
GeneDx RCV001670271 SCV001891310 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001670271 SCV005250678 benign not provided criteria provided, single submitter not provided

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