ClinVar Miner

Submissions for variant NM_005647.4(TBL1X):c.749+15G>A

dbSNP: rs2301675
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001621364 SCV001846462 benign not provided 2019-06-28 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001815594 SCV002062240 benign Hypothyroidism, congenital, nongoitrous, 8 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001621364 SCV005279071 benign not provided criteria provided, single submitter not provided

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