ClinVar Miner

Submissions for variant NM_199334.5(THRA):c.425G>T (p.Arg142Leu)

dbSNP: rs1598396222
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989846 SCV001140437 uncertain significance Congenital nongoitrous hypothyroidism 6 2019-05-28 criteria provided, single submitter clinical testing

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