ClinVar Miner

Submissions for variant NM_198999.3(SLC26A5):c.1312-76G>A

gnomAD frequency: 0.01602  dbSNP: rs72655391
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 RCV001650171 SCV001868596 benign not provided 2018-09-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001650171 SCV005270505 benign not provided criteria provided, single submitter not provided

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