ClinVar Miner

Submissions for variant NM_003466.4(PAX8):c.479-29C>A

dbSNP: rs13015478
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654848 SCV001869265 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788686 SCV002029397 benign Hypothyroidism, congenital, nongoitrous, 2 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001654848 SCV005242621 benign not provided criteria provided, single submitter not provided

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