ClinVar Miner

Submissions for variant NM_178138.6(LHX3):c.*104del

dbSNP: rs146678449
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000371868 SCV000478674 likely benign Combined Pituitary Hormone Deficiency, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001536560 SCV001753337 benign not provided 2018-06-22 criteria provided, single submitter clinical testing

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