ClinVar Miner

Submissions for variant NM_006947.4(SRP72):c.1679-136T>G

gnomAD frequency: 0.02169  dbSNP: rs59110249
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 RCV001537124 SCV001753959 benign not provided 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001537124 SCV005301955 benign not provided criteria provided, single submitter not provided

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