ClinVar Miner

Submissions for variant NM_001190919.2(THRA):c.1130C>T (p.Ser377Leu)

dbSNP: rs137853164
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV001771785 SCV002011714 uncertain significance Congenital nongoitrous hypothyroidism 6 2021-09-23 no assertion criteria provided clinical testing

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