ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.759+20C>T

gnomAD frequency: 0.00315  dbSNP: rs200769484
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
Invitae RCV001523749 SCV001733519 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001523749 SCV001784623 likely benign not provided 2020-06-11 criteria provided, single submitter clinical testing

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