ClinVar Miner

Submissions for variant NM_198999.3(SLC26A5):c.153-10G>A

gnomAD frequency: 0.00143  dbSNP: rs200680274
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 RCV000909661 SCV000726355 benign not provided 2020-07-20 criteria provided, single submitter clinical testing
Invitae RCV000909661 SCV001054478 benign not provided 2024-01-13 criteria provided, single submitter clinical testing

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