ClinVar Miner

Submissions for variant NM_178138.6(LHX3):c.634_636del (p.Glu212del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003990882 SCV004807927 uncertain significance Non-acquired combined pituitary hormone deficiency with spine abnormalities 2024-03-29 criteria provided, single submitter clinical testing

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