ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.949+437del

dbSNP: rs35599379
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001641982 SCV001860896 benign not provided 2019-11-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495976 SCV002806355 benign Glucocorticoid deficiency 5 2021-10-25 criteria provided, single submitter clinical testing

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